CA2284163A1 - Hiv protease inhibitors - Google Patents
Hiv protease inhibitors Download PDFInfo
- Publication number
- CA2284163A1 CA2284163A1 CA002284163A CA2284163A CA2284163A1 CA 2284163 A1 CA2284163 A1 CA 2284163A1 CA 002284163 A CA002284163 A CA 002284163A CA 2284163 A CA2284163 A CA 2284163A CA 2284163 A1 CA2284163 A1 CA 2284163A1
- Authority
- CA
- Canada
- Prior art keywords
- compound
- alkyl
- group
- purity
- pharmaceutically acceptable
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/22—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/36—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/02—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrrole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
HIV protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of the HIV protease enzyme, causing the replication of the HIV virus to terminate. These compounds, as well as pharmaceutical compositions that contain these compounds and optionally other anti-viral agents as active ingredients, are suitable for treating patients or hosts infected with the HIV virus, which is known to cause AIDS.
Description
HIV PROTEASE INHIBITORS
BACKGROUND AND SUMMAR~i' OF THE INVENTION
This invention relates to a novel series of chemical compounds useful as HI:V protease inhibitors and to the use of such compounds as antiviral agents.
Acquired Immune L>eficiency Syndrome (AIDS) is a rela-tively newly recognized disease or condition. AIDS causes a gradual breakdown of the body's immune system as well as progressive deterioration of the central and peripheral nervous systems. Since its initial recognition in the early 1980's, AIDS has spread rapidly and has now reached epidemic proportions within a relatively limited segment of the population. Intensive research has led to the discovery of the responsible agent, human T-lymphotropic retrovirus III
(HTLV-III), now more commonly referred to as the human immunodeficiency virus; or HIV.
HIV is a member c>f the class of viruses known as retroviruses. The ret.roviral genome is composed of RNA
which is converted to DNA by reverse transcription. This retroviral DNA is then stably integrated into a host cell's chromosome and, emplo~~ing the replicative processes of the host cells, produces new retroviral particles and advances the infection to other cells. HIV appears to have a particular affinity for the human T-4 lymphocyte cell which plays a vital role in the body's immune system. HIV
infection of these white blood cells depletes this white cell population. Eventually, the immune system is rendered inoperative and ineffective against various opportunistic diseases such as, among others, pneumocystic carini pneumonia, Kaposi's sarcoma, and cancer of the lymph system.
Although th.e exact mechanism of the formation and work-ing of the HIV virus i.s not understood, identification of the virus has le:d to some progress in controlling the disease. For example, the drug azidothymidine (AZT) has been found effective f:or inhibiting the reverse transcription of the retroviral genome of the HIV virus, SUBSTITUTE SHEET (RULE 26) thus giving a measure of control, though not a cure, for patients afflicted with AIDS. The search continues for drugs that can cure or at least provide an improved measure of control of the deadly HIV virus.
Retroviral replication routinely features post-translational processing of polyproteins. This processing is accomplished by virally encoded HIV protease enzyme.
This yields mature polypeptides that will subsequently aid in the formation and function of infectious virus. If this molecular processing is stifled, then the normal production of HIV is terminated. Therefore, inhibitors of HIV protease may function as anti-HIV viral agents.
HIV protease is one of the translated products from the HIV structural protein pol gene. This retroviral protease specifically cleaves other structural polypeptides at discrete sites to release these newly activated structural proteins and enzymes, thereby rendering the virion replication-competent. As such, inhibition of the HIV
protease by potent compounds may prevent proviral integration of infected T-lymphocytes during the early phase of the HIV-1 life cycle, as well as inhibit viral proteolytic processing during its late stage. Additionally, the protease inhibitors may have the advantages of being more readily available, longer lived in virus, and less toxic than currently available drugs, possibly due to their specificity for the retroviral protease.
In accordance with this invention, there is provided a novel class of chemical compounds that can inhibit and/or block the activity of the HIV protease, which halts the proliferation of HIV virus, pharmaceutical compositions containing these compounds, and the use of the compounds as inhibitors of the HIV protease.
The present invention relates to compounds falling within formula (9) below, and pharmaceutically acceptable salts, prodrugs, and solvates thereof, that inhibit the protease encoded by human immunodeficiency virus (HIV) type 1 (HIV-1) or type 2 (HIV-2). These compounds are useful in the treatment of infection by HIV and the treatment of the-SUBSTITUTE SHEET (RULE 26) acquired immune deficiency syndrome (AIDS). The compounds, their pharmaceutically acceptable salts, and the pharmaceutical compositions of the present invention can be used alone or in combination with other antivirals, immunomodulators, antibiotics or vaccines. Compounds of the present invention ca.n also be used as prodrugs. Methods of treating AIDS, methods of treating HIV infection and methods of inhibiting HIV protease are disclosed.
The compounds of the present invention are of the formula (9):
R
Me O SPh O~N=R' HO , _ H OH N H
H
wherein:
R and R' <~re independently selected from H, a substituted or unsubstituted alkyl-OR1 group, a cycloalkyl group substitui~ed with a (C,-C6) alkyl group or a (C1-C~)alkyl-OH group, a heterocycle group substituted with a (C1-C6) alkyl gr~~up or a (C,-C6) alkyl-OH group, an alkyl-NRzR3 group, or an a:Lkyl-S (X) (Y) R4 group, wherein R1 is H, a. substituted or unsubstituted alkyl group, or an acyl group;
RZ and R3 ;ire each independently selected from H, substituted or mnsubstituted alkyl, cycloalkyl, heterocyc_Le, and aryl groups, and acyl and sulfonyl groups;
Rq is H, a substituted or unsubstituted alkyl, cycloalky~_, het~=_rocycle, or aryl group; and X and Y are each independently selected from =O and nothing;
or a pharmaceut:icall~~ acceptable prodrug, salt or solvate thereof.
SUBSTITUTE SHEET (RULE 26) WO 98/40357 PCTlUS98/04735 Preferably in the compounds of formula 9, R is H. More preferably, R is H and R' is a cycloalkyl group selected f rom CHzOH CH3 CHzOH CHzOH
. and Preferably in the compounds of formula 9 when at least one of R and R' is an alkyl-OR1 group, R, is H. Particularly when at least one of R and R' is an alkyl-OR1 group, the alkyl-ORl is selected from -C (CH3) ZCHZOH, -CH (CH3) CHZOH, -CHzCHzOH, -C (CH3) (CHzOH) 2, -C (CH3) ?-O-CHI-O-CH3, -C (CHI) zCH2-O-CHZ-O-CH3, and -C (CH3) ZCH2-O-acyl, or a pharmaceutically acceptable prodrug, salt or solvate thereof.
Preferably when at least one of R and R' is a cycloalkyl group substituted with a (C,-C6)alkyl group or a (C1-C6)alkyl-OH group, the cycloalkyl group is selected from:
s CH3 ' CH3 _ CH2QH CH3 CHzOH CHzOH
. and Preferably when at least one of R and R' is a heterocycle group substituted with a (C1-C6) alkyl group or a (C1-C6)alkyl-OH group, the heterocycle group is selected from:
H3C H3C HaC C H3 'S
O° S' , S , N /
O ° ~ , C IN-R3> and wherein R3 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group, or an acyl or sulfonyl group.
A preferred species of the formula (9) is [3S-[2(2S*,3S*),3 alpha,4a beta,8a beta]]-N-(1,1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-SUBSTITUTE SHEET (RULE 26) methylbenzoyl)~~mino]-4-(phenylthio)butyl]-3-isoquinolineca:rboxamide H
Me O SPh O~N
~~ OH
H~~ ' Me Me y ~N wN
H ~ H
H
and its pharmaceutically acceptable salts, and its prodrug analogs. Preferred prodrugs can be obtained by replacing the hydrogen in one of the alcohol groups with an acyl group, and more preff~rably an amino acid acyl group.
The present invention further provides pharmaceutical formulations compris_Lng an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier, such as a dilue~nt or excipient.
The present invention further provides a method of treating AIDS compri:~ing administering to a host or patient, such as a primate, an effective amount of a compound of the present invention.
The present invention further provides a method of inhibiting HIV replication comprising administering to an HIV infected cell, a cell susceptible to HIV infection or a host or patient, such as a primate, an effective amount of a compound of the present invention.
Det;~iled Description of the Invention The present invE:ntion provides new compounds falling within formula (9), as described above, that are useful for treating HIV infection and/or AIDS.
Applicants incorporate by reference U.S. Patent No.
5,484,926, U.S. Patent Application Nos. 08/708,411 and 08/708,607, and Japanese Patent Application Nos. JP 95-2481.83 and JP 95-2481.84, with the caveat that the definitions of preferences, terms, variables, labels and the SUBSTITUTE SHEET (RULE 26) like used in each application are applicable only to the corresponding disclosure from that application.
In particular, since each of the above-identified applications incorporated by reference was prepared separately, the original applications may use in some instances the same term, label or variable to mean something different. For example, the variable "X" is used in each application, but each application has its own distinct definition of the substituent or moiety represented by this variable. It will be apparent to those skilled in the art that the terms, labels and variables in each application incorporated by reference are limited solely to the disclosure from that application, and may be replaced by other suitable terms, labels and variables or the like representing the particular substituents and moieties. Of course, those skilled in the art will realize that any suitable set of terms, labels and variables may be used to generically or more specifically represent the subject matter disclosed in the present application, including terms, labels, variables, and the like universally applicable to the incorporated disclosures of the above-identified applications and the following disclosure.
Compounds of the formula (9) may be prodrugs, which can serve to improve the pharmaceutical properties of the compounds, such as pharmacokinetic properties, for example, improved bioavailability or solubility. The preparation of prodrugs may be carried out by standard methods known to those skilled in the art. A preferred prodrug can be obtained by acylation or alkylation of the starting alcohol when R or R' is CH ( CH3 ) ZCHZOH .
All temperatures stated herein are in degrees Celsius (°C). All units of measurement employed herein are in weight units except for liquids which are in volume units.
The term "alkyl" as used herein refers to straight or branched chain groups, preferably, having one to eight, more preferably having one to six, and most preferably having from one to four carbon atoms. The term "C1-C6 alkyl"
represents a straight or branched alkyl chain having from.
SUBSTITUTE SHEET (RULE 26) one to six carbon atoms. Exemplary C1-C6 alkyl groups include methyl,, ethyl, n- propyl, isopropyl, butyl, isobutyl, sec-butyl, t-butyl, pentyl, neo-pentyl, hexyl, isohexyl, and t:he like. The term "C1-C6 alkyl" includes within its def_Lnition the term "C1-CQ alkyl" .
The term "cyclo<~lky1" represents a saturated or partially saturated, mono- or poly-carbocylic ring, preferably having 5-:14 ring carbon atoms. Exemplary cycloalkyls include monocyclic rings having from 3-7, preferably 3-6, carbon atoms, such as cyclopropyl, cyclobutyl, cyc:lopent:yl, cyclohexyl, cycloheptyl and the like. An exemplary cycloalkyl is a C,-C~ cycloalkyl, which is a saturated hydrocarbon ring structure containing from five to seven carbon atoms.
The term "alkoxyl" represents -O-alkyl. An example of an alkoxyl is a C1-C6 alkoxyl, which represents a straight or branched alkyl chain having from one to six carbon atoms attached to an oxygen atom. Exemplary C1-C~ alkoxyl groups include methox:yl, et:hoxyl, propoxyl, isopropoxyl, butoxyl, sec-butoxyl, t-butoxyl, pentoxyl, hexoxyl, and the like.
C1-C6 alkoxyl include; within its definition a C1-Cq alkoxyl.
The term "aryl" as used herein refers to a carbocyclic or heterocyclic, aromatic, 5-14 membered monocyclic or polycyclic ring. Exemplary aryls include phenyl, naphthyl, anthryl, phenan.thryl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, furyl, isothiazolyl, furazanyl, isoxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, benzo[b]thienyl, naphtho[2,3-b]thianthrenyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxathienyl, indolizinyl, isoindolyl, indolyl, indazolyl, purinyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl, quinoxyalinyl, quinzolinyl, benzothiazolyl, benzimidazolyl, tetrahydroquinolinyl, cinnolinyl, pteridinyl, carbazolyl,~
beta-carbolinyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phen.azinyl, isothiazolyl, phenothiazinyl, and phenoxazinyl.
The term "arylox.yl" represents -O-aryl.
SUBSTITUTE SHEET (RULE 26) _g_ The term "hydrolyzable group" is a group, which when bonded to an oxygen, forms an ester, which can be hydrolyzed in vivo to a hydroxyl group. Exemplary hydrolyzable groups, which are optionally substituted, include acyl function, sulfonate function and phosphate function. For example, such hydrolyzable groups include blocked or unblocked amino acid residue, a hemisuccinate residue, and a nicotinate residue.
The term "halogen" represents chlorine, fluorine, bromine or iodine. The term "halo" represents chloro, fluoro, bromo or iodo.
The term "carbocycle" represents an aromatic or a saturated or a partially saturated 5-14 membered monocyclic or polycyclic ring, such as a S- to 7-membered monocyclic or 7- to 10-membered bicyclic ring, wherein all the ring members are carbon atoms.
The term "heterocycle" represents an aromatic or a saturated or a partially saturated, 5-14 membered, monocylic or polycyclic ring, such as a 5- to 7-membered monocyclic or 7- to 10-membered bicyclic ring, having from one to three heteroatoms selected from nitrogen, oxygen and sulfur, and wherein any nitrogen and sulfur heteroatoms may optionally be oxidized, and any nitrogen heteroatom may optionally be quaternized. The heterocyclic ring may be attached at any suitable heteroatom or carbon atom. Examples of such heterocycles include decahydroisoquinolinyl, octahydro-thieno[3,2-c]pyridinyl, piperidinyl, piperazinyl, azepinyl, pyrrolyl, pyrrolidinyl, pyrazolyl, pyrazolidinyl, imidazolyl, isobenzofuranyl, furazanyl, imidazolinyl, imidazolidinyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, thianthrenyl, triazinyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, quinuclidinyl, iso-thiazolidinyl, indolyl, quinolinyl, chromenyl, xanthenyl, isoquinolinyl, benzimidazolyl, thiadiazolyl, benzopyranyl, benzothiazolyl, benzoazolyl, furyl, tetrahydrofuryl, tetrahydropyranyl, thienyl, benzothienyl, benzo[b]thienyl, naphtho[2,3-b]thienyl, thiamorpholinyl, SUBSTITUTE SHEET (RULE 26) thiamorpholiny:Lsulfoxide, thiamorpholinylsulfone, oxadiazolyl, t:riazolyl, tetrahydroquinolinyl, tetrahydriso-quinolinyl, phc~noxathienyl, indolizinyl, isoindolyl, indazolyl, pur:inyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl,, quinoxyalinyl, quinzolinyl, tetrahydroquinolinyl, cinnolinyl, pteridinyl, carbazolyl, beta-carboliny=L, phenanthridinyl, acridinyl, perimidinyl, phenanthroliny=L, phenazinyl, isothiazolyl, phenothiazinyl, and phenoxazinyl.
The term "thioether" includes S-aryl, such as phenylthio and naphtlzylthio; S-heterocycle where the heterocycle is saturated or partially saturated;
S- (CS-C~) -cycloalkyl; and S-alkyl, such as C,-C~ alkylthio.
In the thioether, the=_ -aryl, the -heterocycle, the -cycloalkyl anc~ the --alkyl can optionally be substituted.
An example of a thioether is "C1-C6 alkylthio", which represents a st;raight~ or branched alkyl chain having from one to six carbon atoms attached to a sulfur atom.
Exemplary Cl-C6 alkylthio groups include methylthio, ethylthio, propylthio, isopropylthio, butylthio, sec-butylthio, t-bL~tylth_Lo, pentylthio, hexylthio, and the like.
The term "mercapto" represents -SH.
The term "amino" represents -NL1L2, wherein Ll and LZ
are preferably indepE:ndently selected from oxygen, carbocycle, het.erocyc:le, alkyl, sulfonyl and hydrogen; or NC (0) L3, wherein L3 is preferably alkyl, alkoxyl, hydrogen or -NL~L~. The ar~~l, alltyl and alkoxyl groups can optionally be substituted. A,n example of an amino is C1-C9 alkylamino, which represents a straight or branched alkyl chain having from one to four carbon atoms attached to an amino group.
Exemplary C1-C9 alkylamino groups include methylamino, ethylamino, propylam.i_no, isopropylamino, butylamino, sec-butylamino, and. the 7.ike. Another example of an amino is di(C1-C9)alkylamino, which represents two straight or branched alkyl chain~~, each having from one to four carbon atoms attached to a common amino group. Exemplary di(C1-CQ)alkylamino groups include dimethylamino, ethylmethylamino, met:hylpropylamino, ethylisopropylamino, SUBSTITUTE SHEET (RULE 26) butylmethylamino, sec-butylethylamino, and the like. An example of an amino is C1-Cq alkylsulfonylamino, which has a straight or branched alkyl chain having from one to four carbon atoms attached to a sulfonylamino moiety. Exemplary C1-Cq alkylsulfonylamino groups include methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, isopropylsulfonylamino, butylsulfonylamino, sec-butylsulfonylamino, t-butylsulfonylamino, and the like.
The term "acyl" represents L6C(O)L4, wherein L6 is a single bond, -O or -N, and further wherein Lq is preferably alkyl, amino, hydroxyl, alkoxyl or hydrogen. The alkyl and alkoxyl groups can optionally be substituted. An exemplary acyl is a C1-C~ alkoxycarbonyl, which is a straight or branched alkoxyl chain having from one to four carbon atoms attached to a carbonyl moiety. Exemplary C,-CQ
alkoxycarbonyl groups include methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, and the like. Another exemplary acyl is a carboxy wherein L6 is a single bond and Lq is alkoxyl, hydrogen, or hydroxyl. A further exemplary acyl is N-(C1-C9) alkylcarbamoyl (L6 is a single bond and L4 is an amino) , which is a straight or branched alkyl chain having from one to four carbon atoms attached to the nitrogen atom of a carbamoyl moiety. Exemplary N-(C1-Cq)alkylcarbamoyl groups include N-methylcarbamoyl, N-ethylcarbamoyl, N-propylcarbamoyl, N-isopropylcarbamoyl, N-butylcarbamoyl, and N-t-butylcarbamoyl, and the like. Yet another exemplary acyl is N,N-di(C1-C4)alkylcarbamoyl, which has two straight or branched alkyl chains, each having from one to four carbon atoms attached to the nitrogen atom of a carbamoyl moiety. Exemplary N,N-di(C1-C4)alkylcarbamoyl groups include N,N-dimethylcarbamoyl, N,N-ethylmethylcarbamoyl, N,N-methylpropylcarbamoyl, N,N-ethylisopropylcarbamoyl, N,N-butylmethylcarbamoyl, N,N-sec-butylethylcarbamoyl, and the like.
The term "sulfinyl" represents -SO-L5, wherein LS is preferably alkyl, amino, aryl, cycloalkyl or heterocycle.
SUBSTITUTE SHEET (RULE 26) The alkyl, aryl, cycloalkyl and heterocycle can all optionally be substituted.
The term "sulfonyl" represents -SOz-L5, wherein LS is preferably alkyl, aryl, cycloalkyl, heterocycle or amino.
The alkyl, aryl, cycloalkyl and heterocycle can all optionally be substituted. An example of a sulfonyl is a C1-Cq alkylsulfonyl, which is a straight or branched alkyl chain having from one to four carbon atoms attached to a sulfonyl moiety. Exemplary C1-Cq alkylsulfonyl groups include methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfo:zyl, butylsulfonyl, sec-butylsulfonyl, t-butylsulfonyl ;end the like.
As indical~ed above, many of the groups are optionally substituted. :Ln fact, unless specifically noted, all of the groups defined by the terms defined in this application may be substituted or unsubstituted. For instance, when the term "alkyl" i:~ used, it should be understood to encompass both substituted and unsubstituted alkyl unless specific exclusion of one or the other is positively stated.
Examples of substituents for alkyl and aryl include mercapto, thioether, nitro (NOZ), amino, aryloxyl, halogen, hydroxyl, alko~tyl, and acyl, as well as aryl, cycloalkyl and saturated and partially saturated heterocycles. Examples of substituents for hetE~rocycle and cycloalkyl include those listed above for alkyl and aryl, as well as aryl and alkyl.
Exemplary substituted aryls include a phenyl or naphthyl ring :~ubstii:uted with one or more substituents, preferably one to three substituents, independently selected from halo, hydx-oxy, rnorpholino (C1-CQ) alkoxy carbonyl, pyridyl (C1-C~) alkoxycarbonyl, halo (C1-Cq) alkyl, C1-C9 alkyl, C1-C9 alkoxy, carbox~~, C1-C'q alkoxycarbonyl, carbamoyl, N- (Ci-C9) alkylcarbamo:yl, amino, C1-Cq alkylamino, di (C1-CQ) alkyl amino o:r a group of the formula -(CH2)a-R~ where a is 1, 2, 3 or 4; and ~.~ is hydroxy, C1-C~
alkoxy, carboxy, C1-Cq alkoxycarbonyl., amino, carbamoyl, C1-C9 alkyl amino or d:i (C1-C9) alkyl amino.
Another substituted alkyl is halo(C,-Cq)alkyl, which represents a straight: or branched alkyl chain having from-SUBSTITUTE SHEET (RULE 26) one to four carbon atoms with 1-3 halogen atoms attached to it. Exemplary halo(C1-C9)alkyl groups include chloromethyl, 2- bromoethyl, 1-chloroisopropyl, 3-fluoropropyl, 2,3-dibromobutyl, 3-chloroisobutyl, iodo-t-butyl, trifluoromethyl and the like.
Another substituted alkyl is hydroxy(C1-CQ)alkyl, which represents a straight or branched alkyl chain having from one to four carbon atoms with a hydroxy group attached to it. Exemplary hydroxy(C1-CQ)alkyl groups include hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, 2-hydroxy-isopropyl, 4-hydroxybutyl and the like.
Yet another substituted alkyl is C1-C9 alkylthio(C;-C4) alkyl, which is a straight or branched Cl-C9 alkyl group with a C1-CG alkylthio group attached to it. Exemplary C1-C, alkylthio(C1-Cq)alkyl groups include methylthiomethyl, ethylthiomethyl, propylthiopropyl, sec-butylthiomethyl, and the like.
Yet another exemplary substituted alkyl is heterocycle(C1- C9)alkyl, which is a straight or branched alkyl chain having from one to four carbon atoms with a heterocycle attached to it. Exemplary heterocycle(C1-CQ)alkyls include pyrrolylmethyl, quinolinyl-methyl, 1-indolylethyl, 2-furylethyl, 3-thien-2-ylpropyl, 1-imidazolylisopropyl, 4-thiazolylbutyl and the like.
Yet another substituted alkyl is aryl(C1-Cq)alkyl, which is a straight or branched alkyl chain having from one to four carbon atoms with an aryl group attached to it.
Exemplary aryl(Cl-C9)alkyl groups include phenylmethyl, 2-phenylethyl, 3-naphthyl-propyl, 1-naphthylisopropyl, 4-phenylbutyl and the like.
The heterocycle can, for example, be substituted with 1, 2 or 3 substituents independently selected from halo, halo (C~- CQ ) alkyl , C,-Cq alkyl , C1-C4 alkoxy, carboxy, CI-C9 alkoxycarbonyl, carbamoyl, N-(C,-CQ)alkylcarbamoyl, amino, C1-CQalkylamino, di (C1-CQ) alkyl amino or a group having the structure - (CHZ) a-R' where a is 1, 2, 3 or 4 and R' is hydroxy, C2-CQ alkoxy, carboxy, C1-Cq alkoxycarbonyl, amino, carbamoyl, C1-Cq alkyl amino or di (C,-C4) alkylamino.
SUBSTITUTE SHEET (RULE 26) Examples of substituted heterocycles include 3-N-t-butyl carboxam.ide decahydroisoquinolinyl, 6-N-t-butyl carboxamide octahydro-thieno[3,2-c]pyridinyl, 3-methylimidazolyl, 3-methoxypyridyl, 4-chloroquinolinyl, 4-aminothiazolyl, 8-methylquinolinyl, 6-chloroquinoxalinyl, 3-ethylpyridyl, 6-methoxybenzimidazolyl, 4-hydroxyfuryl, 4-methylisoqui:aolinyl, 6,8-dibromoquinolinyl, 2-methyl-1,2,3,4-tetrahydroisoquinolinyl, N-methyl-quinolin-2-yl, 2-t-butoxycarbc~nyl-1,2,3,4-isoquinolin-7-yl and the like.
Exemplary heterocyclic ring systems represented by A or B include (1) !~-membered monocyclic ring groups such as thienyl, pyrro:lyl, ivmidazolyl, pyrazolyl, furyl, isothiazolyl, :Euraza:nyl, isoxazolyl, thiazolyl and the like;
(2) 6-membered monocyclic groups such as pyridyl, pyrazinyl, pyrimidinyl, p~~ridazinly, triazinyl and the like; and (3) polycyclic hete~rocyc:lic rings groups, such as decahydroisoquinolinyl, octahydro-thieno [3,2-c] pyridinyl, benzo [b] thieny:L , naphtho [2 , 3 -b] thianthrenyl , isobenzofurany:L,_chromenyl, xanthenyl, and fully or partially saturated analogs thereof.
A cycloallcyl ma~~ be optionally substituted with 1, 2 or 3 substituents indepE=_ndently selected from halo, halo (C~-C~) alky:L, C1-C9 alkyl, C1-Cq alkoxy, carboxy, C1-C4 alkoxycarbonyl , carbamoyl , N- ( C, -CQ ) alkyl carbamoyl , amino , Cl-Cq alkyl amino, di (Ci-C~) alkylamino or a group having the structure - (CH2) a-R' where a is 1, 2, 3 or 4 and R' is hydroxy, Cl-C9 alkoxy, carboxy, C1-Cq alkoxycarbonyl, amino, carbamoyl, Cz-C9 alkylamino or di (C,-C9) alkyl amino.
Exemplary substituted cycloalkyl groups include 3-methylcyclopE:ntyl, 4-ethoxycyclohexyl, 5-carboxycyclo-~hepty:L, 6-chlorocyclohexyl and the like.
Exemplary substituted hydrolyzable groups include N-benzyl glycyl., N-Cbz-L-valyl, and N-methyl nicotinate.
The compounds of the present invention have at least five asymmetric: centers denoted by an asterisk in the formula (9) below:
SUBSTITUTE SHEET (RULE 26) SPh Me O Oa-N:R
HO N** N
H OH H
H
As a consequence of these asymmetric centers, the compounds of the present invention can occur in any of the possible stereoisomeric forms, and can be used in mixtures of stereoisomers, which can be optically active or racemic, or can be used alone as essentially pure stereisomers, i.e., at least 95% pure. All asymmetric forms, individual stereoisomers and combinations thereof, are within the scope of the present invention.
The individual stereoisomers may be prepared from their respective precursors by the procedures described above, by resolving the racemic mixtures, or by separating the diastereomers. The resolution can be carried out in the presence of a resolving agent, by chromatography or by repeated crystallization or by some combination of these techniques which are known in the art. Further details regarding resolutions can be found in Jacques et al., Enantiomers, Racemates, and Resolutions, John Wiley & Sons 1981.
Preferably, the compounds of the present invention are substantially pure, i.e, over 50o pure. More preferably, the compounds are at least 75% pure. Even more preferably, the compounds are more than 90% pure. Even more preferably, the compounds are at least 95% pure, more preferably, at least 97o pure, and most preferably at least 99o pure.
As mentioned above, the invention includes the pharmaceutically acceptable salts of the compounds defined by formula (9). A compound of this invention may possess a sufficiently acidic, a sufficiently basic, or both functional groups, and accordingly react with any of a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.
SUBSTITUTE SHEET (RULE 26) The term "pharmaceutically acceptable salt", as used herein, refers to salts of the compounds of the above formula which ;ire substantially non-toxic to living organisms. Exemplary pharmaceutically acceptable salts include those ;alts prepared by reaction of the compounds of the present im;rention with a mineral or organic acid or an inorganic base. The reactants are generally combined in a mutual solvent such .as diethylether or benzene, for acid addition salts,, or water or alcohols for base addition salts. The sa_Lts normally precipitate out of solution within about one hour to about ten days and can be isolated by filtration or other conventional methods. Such salts are known as acid addition and base addition salts.
Acids that: may be employed to form acid addition salts are inorganic ciCldS such as hydrochloric acid, hydrobromic acid, hydroiod~_c acid, sulfuric acid, phosphoric acid, and the like, and organic acids such as p-toluenesulfonic, methanesulfonic: acid,, oxalic acid, p-bromophenylsulfonic acid, carbonic acid, succinic acid, citric acid, benzoic acid, acetic acid, and the like.
Examples of pharmaceutically acceptable salts are the sulfate, pyrosulfate, bisulfate, sulfite, bisulfate, phosphate, monohydroc~enphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, propionate, decanoate, caprylate, acrylate, formate, isobutyrate, caproate, heptanoate, propiolate, oxalate, malona.te, succinate, suberate, sebacate, fumarate, maleate, butyne-1,4-c~ioate, hexyne-1,6-dioate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, phthalate, sulfonate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutyrate, citrate, lactate, g-hydroxybutyrate, glycollate, tartrate, methane-sulfonate, propanesulfonate, naphthalene-1-sulfonate, napththalene-2-sulfonate, mandelate and the like.
Preferred pharmaceutically acceptable acid addition salts are those formed with mineral acids such as hydrochloric acid anal hydrobromic acid, and those formed SUBSTITUTE SHEET (RULE 26) with organic acids such as malefic acid and methanesulfonic acid.
Base addition salts include those derived from inorganic and organic bases, such as ammonium or alkali or alkaline earth metal hydroxides, carbonates, bicarbonates, and the like. Such bases useful in preparing the salts of this invention thus include sodium hydroxide, potassium hydroxide, ammonium hydroxide, potassium carbonate, sodium carbonate, sodium bicarbonate, potassium bicarbonate, calcium hydroxide, calcium carbonate and the like. The potassium and sodium salt forms are particularly preferred.
A "pharmaceutically acceptable prodrug" is intended to mean a compound that may be converted under physiological conditions or by solvolysis to a compound of the formula 9.
A "pharmaceutically acceptable solvate" is intended to mean a solvate that retains the biological effectiveness and properties of the biologically active components of compounds of formula 9.
Examples of pharmaceutically acceptable solvates include, but are not limited to, compounds of formula 9 in combing ion with water, isopropanol~, ethanol, methanol, DMSO, ethyl acetate, acetic acid, or ethanolamine.
It should be recognized that the particular counterion forming a part of any salt of this invention is not of a critical nature, so long as the salt as a whole is pharmacologically acceptable and as long as the counterion does not contribute undesired qualities to the salt as a whole.
SUBSTITUTE SHEET (RULE 26) A preferred compound is compound 21 H
Me O sPh O~N
~~ OH
HO - Me Me 1 \ ~N N
lI H OH H
H
[3S- [2 (2S*, 3S* ) , 3 alpha, 4a beta, 8a beta] ] -N- (1, 1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino)-4-(phenylthio)butyl]-3-isoquinolinecarboxamide.
A process for making compound 21 is provided below.
Compound 21 ha:~ also been obtained as a metabolite from the plasma of patients administered [3S-(3R,4aR*,8aR*,a?'S*,3'S*)]-2-[2'-hydroxy-3'-phenylthiomethyl-4' -aza-5' -oxo-Vii' - (2 " -methyl-3 "-hydroxyphenyl) pentyl]
decahydroisoquinolinc=_-3-N-t-butylcarboxamide methanesulfonic acid salt, which is disclosed in U.S. Patent No. 5,484,926.
The compounds o:E formula 9 can be prepared according to the following F:eaction Scheme I.
SUBSTITUTE SHEET (RULE 26) REACTION SCHEME I
Scheme I. General Synthetic Pathway for the Production of 96 and Derivatives R
CONHt-Bu OOOH COOH R R~ Oy N' R' aqums H' N H Mdto~s H' N H Ami~ePrdedon ~~ N . H ' H Rp~ N
--w ----s H
H Step la H Step Ib H
Artidecwpiog H
Step 1 to 2a 2b Rp =artcx prteauggoup 3 SPh R
CbzHN~CI R R
O~N R SPh O tV SPh O~N,R, H.N OH 5 ~_ 'R~ Chrrertnval H CHotoarohol qty N ~ H_N~N
L~proteaon ~ OFI H OH ~H
H epoxide Step xI~lIS
Step 3 cbse-open seqmrce H H
q 6 Step 4 Me AcO~COQ R R
Me p SPh O~ N, R, Me O SPh O~ N, R
acetate g Ac0 ~ ~' mmval NFI Y 'N HO ~ ~
H NH Y 'N
antis coplo~ OH ~ OH H
Step 6a H~ ~eP 66 9a H
9b Compound 1a, perhydroisoquinoline, which is commercially available from NSC Technologies (Chicago, IL) or Procos SpA (Milan, Italy) is subjected to prolonged acid hydrolysis in step 1a to obtain compound 2a. A variety of inorganic acids may be used in either an aqueous/organic solvent mixture or in water alone at temperatures above 50 °C. An example of such an inorganic acid is 6N aqueous HCl.
Substitutes for compound la include the corresponding esters lb, thioesters lc or other amides ld:
H COOZ H COSZ CONZ~ZZ
H
H H
H
H ~ ~ H
lb lc ld , where Z, Z1 and Zz may each independently be alkyl, cycloalkyl, heterocycle, or aryl.
SUBSTITUTE SHEET (RULE 26) Compound 2~~ is then protected at the amine nitrogen to obtain compound 2b in step Ib. The protecting group Rp is defined as a suitably conjugating group to avoid unwanted decomposition oi= activated carboxylate derivatives of compound 2b in ~>tep 2. Such protecting groups typically can be carbamate in origin, having a general structure of formula 11:
O
R"O~
The identity of R" in formula 11 can be any alkyl, cycloalkyl, aryl, or heterocycle which can be removed easily in a deprotection step after Step,2. Examples of R"
include, but are not limited to methyl, ethyl, propyl, isopropyl, n-butyl, i:~obutyl, t-butyl or higher branched or unbranched alkyl, 2,2,2-trichloroethyl, 2-trimethylsilylethyl, allyl, phenyl, substituted phenyl, benzyl, substituted benzyl, 9-fluorenylmethyl, 9-anthrylmethyl anal higher polycyclic aromatic ring system.
The following materials, as defined below, can be obtained from the Aldrich Chemical Co. (Sigma Aldrich Fluka):
a 2.2,2-trichloroethyl= -a-12-C-a a H a~3 2-trimethylsllylethyl= -~2-C-SI--a'13 H a-13 allyl= -a-IZ-CH=Cii2 henzyl= _ q.~ / \
9-flourenylmethyl =
I
9-anihrylnethyt =
SUBSTITUTE SHEET (RULE 26) Such protecting groups typically can be installed by an acylation reaction of the corresponding haloformate ester 12a or a dicarbonate 12b:
O O
I~'O~X R"O~Y
12a 12b X = halogen Y = OCOR"
in the presence of a suitable base in typical organic solvents for these types of reactions such as halogenated solvents, ethers and hydrocarbons. Such bases are typically inorganic, such as metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, 1,8-diazabicyclo[2.2.2)octane (DABCO) or related di- or trialkyl-amines, as well as amidine bases like 1,8-diazabicyclo [5.4 . 0) under-7-ene (DBU) and 1, 8-diazabicyclo[4.3.0]non-5-ene (DBN). The following materials, as defined below, can be obtained from the Aldrich Chemical Co. (Sigma Aldrich Fluka):
~aaoo =
oBU = ~~
These reactions are typically run anywhere from below room temperature to approximately 100 °C.
The amide coupling Step 2 can be accomplished in any number of fashions depending on how the carboxyl group is activated. A group J is installed in Step 2 by reaction of the carboxylic acid 2b to produce the activated derivative 2c.
SUBSTITUTE SHEET {RULE 26) Sten 2 J R
COOH 05! I
activaW nofthe Rpm R~N~R O~ N~R
N H carboxyl goup N H H ~~ N
-----~ H
H H ~ base H
2b Rp = am~e protect~g goy 2c J = leav~g goup 3 The group ~T can be any of a variety of leaving groups such as alkoxy, hydroxy, halogen, pseudohalogen (including azide, cyanide, isocy<~nate and isothiocyanate), alkyl or arenesulfonate, aromatic heterocycle(bonded through a heteroatom) and N-hyd:roxyheterocycle, including hydroxysuccinimide or hydroxybenzotriazole ester. The following definitions apply to the terms above:
azide -N-t~N
cyanide -C=N
isocyanate-N=C=O
isothiocyanate-t~~g O
alkylsulfonate-O-S-alkyl i O
O
ii arenesuNonate-O-S-aryl O
N-hydroxyhe:erocyclic HO-where N~ = nitrogen heterocycle \~/O\\
N-hydroxysuccinimide HO-N
O
hyd roxybe nnotriazo le ~I N
N
OH
SUBSTITUTE SHEET (RULE 26) The aryl halides (2c, J = halogen) may be prepared using inorganic halogenating agents such as thionyl chloride or bromide, phosphorous trichloride or bromide, phosphorous pentachloride or bromide or organic agents such as oxalyl chloride or trichlorisocyanuric acid. Esters (2c, J = OR") (R" is defined above) may be prepared in a variety of ways starting from the acid chloride 2c where J is Cl by combination with the desired alcohol in the presence of an organic or inorganic base stated previously for the acylation of compound 12a or compound 12b. Alternatively, the ester may be produced by acid-promoted esterification in the presence of the desired alcohol. The sulfonates (2c, J =
OSO~Wl, where Wl is alkyl or aryl) are typically made by reaction of the carboxylic acid 2b with alkyl or arylsulfonyl chlorides in the presence of an organic amine base such as triethylamine in a non-polar solvent at temperatures below 0 °C. Alkyl and arylsulfonyl are defined as follows:
alkylx~lfonylchloride = d-S-alkyl O
O
arenesulfonyl chloride = d-S-aryl O
The pseudohalogen derivatives of 2c (J = pseudohalogen) are typically made from the acid halides 2c (J = halogen) by reaction with inorganic pseudohalide in the presence of a base. Such bases include, but are not limited to metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, 1,8-diazabicyclo[2.2.2]octane (DABCO) or related di- or trialkylamines, as well as amidine bases like 1,8-diazabicyclo[5.4.0]under-7-ene (DBU) and 1,8-diazabicyclo[4.3.0]non-5-ene (DBN). A particularly preferred base is triethylamine. The heteroaromatic SUBSTITUTE SHEET (RULE 26) derivatives of 2c are also made from the acid halides 2c (J
- halogen), utilizing the specific heteroaromatic compound in the presence of an amine base in a non-polar solvent.
The N-hydroxyher_erocyclic derivatives of 2c can be made from the acid halide; as above and may also be generated using alkyl carbodiim:ides (.alkyl-N=C=N-alkyl, where the alkyl groups can be the same or different) or aryl carbodiimides (aryl-N=C=N-ary:L, where the aryl groups can be the same or different) and an amine base as condensing agents.
The primar~r or secondary amine (shown above the arrow in Step 2 of Scheme I,? used in the coupling process may incorporate suitable protecting groups, depending on the functionality present in the amine and the mode of coupling used. The mode of coupling of 2c with a primary or secondary amine can bE=_ carried out in a variety of ways depending on the' ident=ity of J. 4~Then a free acid is used (2c, J = OH) the. coupling can be performed using carbodiimide-ba~~ed methods utilizing any of the common reagents of thi:~ clas:~, including dicyclohexylcarbodiimide or related dialk:ylcarbodiimides, EDC (salts of 1- (3-dimethylaminopropyl)-.3-ethylcarbodiimide) or related water-soluble reagent; along with an organic amine base in polar organic solvent; such as dioxane, DMF, NMP and acetonitrile in the presence of an N-hydroxyheterocyclic compound such as N-hydroxysuccini.mide or 3-hydroxybenzotriazole.
Alternatively, halofox°mate esters, such as 12d, may be used to temporarily a.ctivat:e the acid to give mixed anhydrides of general formula 2d.
O~OR"
O:yO
R~~N- O
H
R"O~ X
H' 12d X = halogen 2d SUBSTITUTE SHEET (RULE 26) Such haloformate esters are typically as shown in 12d above and include methyl-, ethyl-, isopropyl-, isobutyl-, n-butyl, phenyl- and related alkyl and aryl chloroformates, defined below.
alkyl chloiofortnate = 'I
alkyl-O~Q
O
aryl chlorofortnate = aryl-O~C!
Formula 2d is a possible intermediate in the step from formula 2b to formula 3. Formula 2d is an intermediate, but the process described here results in formula 3, without isolation of Formula 2d.
These reactions are typically performed in a variety of non-polar organic solvents like halocarbons and ethers such as diethyl ether, methyl t-butylether, diisopropyl ether, dioxane and THF at temperatures below 0 °C accompanied by an organic amine base such as triethylamine, diethylamine, diethyl isopropylamine, DABCO or related di- or trialkylamines, as well as amidine bases like DBU and DBN.
When J in compound 2c is an alkyl or arenesulfonate (J
- OSOZR or OSO2Ar), the coupling can be performed in a variety of non-polar organic solvents like halocarbons and ethers, such as diethyl ether, methyl t-butylether, diisopropyl ether, dioxane and THF at temperatures below 0 °C, accompanied by an organic amine base such as triethylamine, diethylamine, diethyl isopropylamine, DABCO
or related di- or trialkylamines, as well as amidine bases like DBU and DBN.
When J in compound 2c is a halogen or pseudohalogen, the coupling may be performed in most common organic solvents such as THF, diethyl ether, dioxane, methyl t-butyl ether or other ethers; acetone, cyclohexanone, methyl isobutylketone and other ketones; esters such as ethyl, SUBSTITUTE SHEET (RULE 26) methyl and isopropyl acetate; halogenated solvents such as halogenated metlzanes and ethanes, chlorobenzene and other halogenated ben:~enes; nitrites such acetonitrile and propionitrile; :Lower alcohols such as ethanol, isopropanol, t-butanol and related alcohols; and polar organic solvents such as dimethy:Lformamide, dimethylsulfoxide, N-methyl-2-pyrrollidone and related amide-containing solvents. A base is frequently used and may be any of a number of inorganic bases such as metal hydroxides, bicarbonates and carbonates or organic baser such as amines like triethylamine, diethylamine, d~_ethyl isopropylamine, DABCO or related di-or trialkylamines, as well as amidine bases like DBU and DBN.
One skillecL in the art will be able to perform the amide coupling ~~tep 2 with other possible J groups.
In Step 3 protect=ing group removal can be accomplished using any of the standard methods for deprotecting a particular clas:~ of protecting group. Simple alkyl- and substituted alk~.Tl~carbamates can be removed with aqueous solutions of ba:>e at t=emperatures up to about 100 °C, employing any of: the common inorganic metal hydroxides such as sodium-, litriium-, potassium- or barium hydroxide or hydroxides of other metals in at least stoichiometric amounts. Carbamate protecting groups that contain benzyl groups bonded tc> oxygen may be removed by hydrogenolysis with a palladium or platinum catalyst. Alternatively, aqueous base hycLrolysis may be used at temperatures up to about 100 °C, employing any of the common inorganic metal hydroxides such as sodium-, lithium-, potassium- or barium hydroxide or hydroxides of other metals in at least stoichiometric a.mount~~. A variety of anhydrous acids may also be used for deprotection of benzyl-based carbamates, including HCl, H:Br and HI. Lewis acids of boron and aluminum such as A1C13, BBr3, BClj in non-polar solvents are also effective. Certain substituted benzyl, aryl or alkyl groups in which the specific substitution pattern is chosen for its ability to be removed under specific conditions may also be used. F'or example, the 2-SUBSTITUTE SHEET {RULE 26) trimethylsilylethylcarbonyl group (Teoc) is a protecting group designed to take advantage of the specific reactivity of the 2-trimethylsilylethyl group in the deprotection process. 2-Trimethylsilylethylcarbonyl chloride may be used to protect the amine nitrogen and may later be removed using sources of fluoride ion such as HF or tetraalkylammonium fluoride salts.
In Step 4, the perhydroisoquinoline piece of formula 4 is connected to the Chloroalcohol (compound 5, Scheme I) via an epoxide intermediate (13) generated via the base-induced closure of the vicinal chlorohydrin functionality.
SPh CbzHN
O
Compound 5 is produced by Kaneka Industries, Japan. Several close-open procedures in proceeding from compound 5 compound 13 ~ compound 6 may be used. The epoxide 13 may be isolated or it may be reacted with 4 added either subsequent to formation of 13 or 4 may be present from the beginning of the sequence. The epoxide 13 can be generated using inorganic bases such as metal hydroxides, carbonates and bicarbonates in solvents such as alcohols like methanol ethanol or isopropyl alcohol, ethers such as THF and dioxane or mixtures of the two. The epoxide can also be generated in a 2-phase solvent system consisting of water and a halocarbon solvent such as dichloromethane along with the base. A phase-transfer catalyst such as a tetraalkylammonium salt may be used to facilitate the process. The process of opening the epoxide 13 with compound 4 is accomplished in alcohol solvents or mixtures of an alcohol and another solvent which may be an ether or a Bipolar aprotic solvent such as dimethylformamide or dimethylsulfoxide. The opening of the epoxide 13 with SUBSTITUTE SHEET (RULE 26) compound 4 to give compound 6 is optimally performed over a period of 2-7 hours at. 50 - 60 °C.
In Step 5 t:he car_bobenzyloxy group can be removed to give the free amine 7.. This can be done using HBr in acetic acid using cosol.vents such as halocarbons. It can also be performed using halide's of boron such as BBrj and BC13 or alkyl substituted boron halides such as dimethylboron bromide in halocarbon solvents like chloroform and dichloromethane at temperatures ranging from 0 °C up to ambient temperature. Alternatively, the carbobenzyloxy group can be removed by hydrolysis using aqueous/alcoholic solutions of metal hydroxides like barium, sodium, lithium or potassium hydroxide at temperatures above ambient for periods of hours.
Step 6a is the coupling of benzoic acid derivatives of formula 8 to give 9a. In Formula 8, Q can be a leaving group. Q can be any of: the leaving groups discussed above for Group J. The compounds of formula 8 where Q = OH or Cl are commercially available from EMS Dottikon, Lenzburg, Switzerland and Sugai Chemical Industries, Ltd. in Japan.
The coupling can be carried out in a variety of ways, depending on the identity of Q. When a free acid is used (Q
- OH), the coupling ca.n be performed using carbodiimide based methods utilizing any of the common reagents of this class including dicyclohexylcarbodiimide or related dialkylcarbodiimides, EDC (salts of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide) or related water soluble reagents along with an organic amine base in polar organic solvents such as dioxane, DMF, NMP and acetonitrile in the presence of an N-hydroxyheterocyclic including N-hydroxysuccinimide or 3-hydroxybenzotriazole. When Q = a halogen or pseudohalogen, the coupling may be performed in most common organic solvents such as THF, diethyl ether, dioxane, methyl t-butyl ether or other ethers; acetone, cyclohexanone, methyl isobutylketone and other ketones;
esters such as ethyl, methyl and isopropyl acetate;
SUBSTITUTE SHEET (RULE 26) halogenated solvents such as halogenated urethanes and ethanes, chlorobenzene and other halogenated benzenes;
nitrites such acetonitrile and propionitrile; lower alcohols such as ethanol, isopropanol, t-butanol and related alcohols, and polar organic solvents such as dimethylformamide, dimethylsulfoxide, N-methyl-2-pyrrollidone and related amide-containing solvents. A base is frequently used and may be any of a number of inorganic bases such as metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, DABCO or related di-or trialkylamines, as well as amidine bases like DBU and DBN.
Acetate removal is accomplished in step 6b with aqueous or alcoholic solutions of inorganic bases such as metal hydroxides, carbonates and bicarbonates at ambient temperatures up to 100 °C. If there is a protected functionality on the carboxamide group bonded to the perhydroisoquinoline ring system, it is best removed at this point (during or after step 6b). The, nature of this step is dependent on the exact identity of the protecting group.
A preferred method for accomplishing the entire process shown in Scheme I is shown in Scheme II.
The Cbz-protected amino acid 15 was coupled with the amine 22 to give the amide 16. The Cbz group was removed by hydrogenation to SUBSTITUTE SHEET (RULE 26) Scheme 11. Synthesis of Amidc 21 H ~ H
I
H COM-I-t-Bu COOIH ~l7 fMS
OII
N 1. 6 N aq. HC1 ~ N H=N ~ ~~ H2 H Me H -~. H ~ N 5% Pd~C 1 N H
H
2. CI~I H FDC, f-Ipgt~H20 H EtOH
H
Pattptltnisoquinoune STEP A STEP 8 -STEP C "
sPh Me C» CI SPh p~ 1V H ~ I \ COC1 OH ~ _ ()I1 SPh N
Me 50°/ aq. thpt-1 ~ pl I ~ 20 CLlotvalaohd Cbal W N H
OH HzN N
IJaCXI, IPA H IPA ~ ~i fi Et3N, THF, EtOH;
Ij ~ then 50%aq. N~OII
STEP D '8 STEP E '9 STEP F
H
SPh Me Oti H OH N . H
H
give the amine :L7. This was coupled with the chloroalcohol via the epoxide using the in situ procedure to give the adduct 18. Com~entional deprotection with base and coupling of the free primary amine with the acid chloride 20 gave rise to amide 2:1. Details of this process are provided below in ExamplE~s 1 A to F. The lettering A to F in Scheme II corresponds i.o Examples 1 A to F below.
The following Examples illustrate aspects of the invention. There examples are for illustrative purposes and are not intended to limit the scope of the invention.
Abbreviations for the terms melting point, nuclear magnetic resonance spectra, electron impact mass spectra, field desorption mass spectra, fast atom bombardment mass spectra, infrared spectra, ultraviolet spectra, elemental analysis, high performance liquid chromatography, and thin layer chromatography are, respectively, m.p., NMR, EIMS, MS(FD), MS(FAB), IR, W, Analysis, HPLC, and TLC. In addition, the absorption maxima listed for the IR spectra are those of ini=erest, not all maxima observed.
SUBSTITUTE SHEET (RULE 26) In conjunction with the NMR spectra, the following abbreviations are used: singlet (s), doublet (d), doublet of doublets (dd) , triplet (t) , quartet (q) , multiplet (m) , doublet of multiplets (dm), broad singlet (br.s), broad doublet (br.d), broad triplet (br.t), and broad multiplet (br.m). J indicates the coupling constant in Hertz (Hz).
Unless otherwise noted, NMR data refer to the free base of the subject compound.
NMR spectra were obtained on a General Electric QE-300 300MHz instrument. Chemical shifts are expressed in b values in ppm. Mass spectra were obtained on a VG ZAB-3 Spectrometer at the Scripps Research Institute, La Jolla, CA. Infra-red spectra were recorded on a Midac Corporation spectrometer. UV spectra were obtained on a Varian,Cary 3E
instrument. Thin layer chromatography was carried out using silica plates available from E. Merck. Melting points were measured on a Mettler FP62 instrument and are uncorrected.
Example 1 Procedures for the Synthesis of Amide of Formula 21 [3S- [2 (2S*, 3S*) , 3 alpha, 4a beta, 8a beta] ] -N- (l, 1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-(phenylthio)butyl]-3-isoquinolinecarboxamide H
SPh O N
Me O ~ ~OH
HO ~ Me Me N
H OH
i A. Perhydroisoquinoline (26.4 g, 111 mmol} (commerically available from NSC Technologies (Chicago, IL) or Procos SpA
(Milan, Italy)) was suspended in water (200 mL) and concentrated aqueous HC1 (200 mL). This mixture was heated SUBSTITUTE SHEET (RULE 26) to reflux and stirred for 3 days, during which time it went into solution. The solvents were removed under reduced pressure to give a light yellow solid. The solid was slurried in 2-propanol (200 mL) and filtered. The filtrate was evaporated under reduced pressure to an oil. EtOAc (100 mL) and water (100 mL) were added and the pH of the solution was brought to 8.0 by the addition of 2 N aqueous KOH.
Benzyl chloroformate (15.8 mL, 111 mmol) was added dropwise over 30 minutes and the pH was kept between 7 and 8 by the addition of 2 N aqueous KOH. The mixture was stirred at room temperature for 18 hours. EtOAc (200 mL) was added and the organic layer was washed with 1 N aqueous HC1 (100 mL), and brine (100 mL). The organic layer was dried (MgS09), filtered, and evaporated under reduced pressure to an oil.
The product was purified by silica gel chromatography, eluting with 1:1 40-60 petroleum ether/EtOAc followed by 1000 EtOAc. The fractions containing product were collected and evaporated under reduced pressure to give the compound 15 (11.3 g, 32%) as a colorless oil: 1H NMR (300 MHz, CDC13) ~ 7.43-7.28 (m, 5 H), 5.17 (br s, 2 H), 4.76 (m, 1 H), 3.79 (m, 1 H), 3.33 (m, 1 H), 2.19 (m, 1 H), 1.96 (m, 1 H), 1.88-1.15 (m, 10 H) .
B. 1-Hydroxyb~~nzotriazole (4.2 g, 31.4 mmol) and EDC (6.0 g, 31.4 mmol) ware added to a solution of acid 15 (8.3 g, 26.2 mmol) in DI~IF (128 mL) at ambient temperature. The mixture was hea":,ed at 80° C for 10 minutes. 1,1-Dimethyl-2-trimethylsilylo:Kyethylamine (5.1 g, 31.4 mmol, prepared from 1,1-dimethyl-2-lzydroxyethylamine (Aldrich Chemical Co.) and hexamethyldisil;~zane (Aldrich Chemical Co.)) by heating the mixture neat under reflux for several hours followed by evaporation of the volatile components was added and the solution was he~~ted at 80° C for 17 hours. The yellow solution was po~ired into EtOAc (250 mL) and 2 N aqueous HCl (250 mL). Afte:r stirring for 10 minutes EtOAc (750 mL) was added and the mixture was washed with H20 (3 x 500 mL) and brine (1 x 250 mL). The combined aqueous layers were extracted with 7~tOAc (1 x 250 mL). The combined organic layers were dried (NazS04) and purified by flash SUBSTITUTE SHEET (RULE 26) chromatography (50/50 EtOAc/hexanes) to give the compound 16 as a colorless oil (7.9 g, 78%): 1H NMR (300 MHz, CD30D) S
7.36 (m, 5 H), 5.20 (d, J = 8.1 Hz, 1 H), 5.10 (m, 1 H), 4.53 (m, 1 H), 3.78 (dd, J = 13.2, 4.4 Hz, 1 H), 3.60 (m, 2 H), 3.48 (d, J = 10.7 Hz, 1 H), 2.15-1.25 (m, 12 H), 1.31 (s, 3 H) , 1.29 (s, 3 H) .
C. A mixture of carbamate 16 (7.9 g, 20.4 mmol) and 5%
palladium on carbon (Pd/C)(1.6 g) was hydrogenated at 50 psi H~ in absolute EtOH (110 mL) at ambient temperature for 18 hours. The mixture was filtered through Celite and evaporated in vacuo to give amine 17 as a white, crystalline solid: 'H NMR (300 MHz, CD30D) b 3.63 (q, J = 7.0 Hz, 2 H), 3.34 (m, 1 H), 3.27 (dd, J = 11.8, 3.3 Hz, 1 H), 2.91 (m, 1 H), 2.02-1.15 (m, 12 H), 1.32 (s, 3 H), 1.31 (s, 3 H).
D. Aqueous 10.2 N NaOH (2.4 mL, 24.5 mmol) was added to a warm (27 °C) suspension of chloroalcohol (obtained from Kaneka Industries in Japan)(10.4 g, 28.6 mmol) in isopropanol (IPA)(104 mL) with mechanical stirring. After 1 hour 1 N aqueous HC1 in IPA (prepared by addition of 1 mL of concentrated aqueous HCl to 12 mL of IPA) approximately (ca.) 1 mL) was added to neutralize (pH = 7). Amine 17 (5.2 g, 20.4 mmol) was added as a solution in IPA (50 mL) and the thin suspension was heated at 60° C for 10 hours. The IPA
was removed in vacuo. The residue was diluted with EtOAc (150 mL) and washed with Hz0 (2 x 50 mL) , saturated aqueous NaHC03 (1 x 50 mL), and brine (1 x 50 mL). The combined aqueous layers were extracted with EtOAc (1 x 25 mL). The combined organic layers were dried (NazSO~) and purified by flash chromatography (75/25 EtOAc/hexanes, then EtOAc) to give the compound 18 as a white solid (8.98 g, 76%): 1H NMR
(300 MHz, CD30D) d 7.33 (m, 10 H) , 5.08 (AB, JAB = 12.2 Hz, ~uAB = 12.1 Hz, 2 H), 3.96, (m, 2 H), 3.56 (q, J = 7.3 Hz, 2 H), 3.50, (m, 1 H), 3.20 (dd, J = 13.6, 9.2 Hz, 1 H), 3.03 (m, 1 H) , 2.64 (m, 2 H) , 2.20-1.20 (m, 14 H) , 1.28 (s, 6 H) .
SUBSTITUTE SHEET (RULE 26) E. 50% aqueous NaOH (2.7 g, 1.8 mL, 33.6 mmol) was added to a suspension of carbamate 18 (6.75 g, 11.6 mmol) in IPA
(34 mL) at ambient temperature. The mixture was heated under reflux for 12 hours. After cooling to ambient temperature, the mixture was diluted with methyl t-butyl ether (MTBE) (600 mL) and washed with H20 (2 x 250 mL) and brine (1 x 125 mL). T'he combined aqueous layers were extracted with MTBE (1 x 150 mL). The combined organic layers were dried (Naz;509) and evaporated in vacuo to give a mixture of compound 19 and benzyl alcohol as an oily white solid: -H NMR 0300 MH:z, CD30D) b 7.34 (m, 10 H) , 4.63 (s, 2 H), 3.81 (m, 1 H), 3.58 (m, 3 H), 3.03-2.60 (m, 5 H), 2.17 (m, 1 H) , 2.05 ('m, 1 H) , 1.87-1.05 (m, 12 H) , 1.30 (s, 3 H) , 1.28 (s, 3 H) .
F. Triethylami:ne (3.2 g, 4.3 mL, 31.2 mmol) was added to a solution of the mixture of amine 19 (4.7 g, 10.4 mmol theory from 18) and benzyl alcohol in EtOH (23 mL) at ambient temperature. A solution of 3-acetoxy-2-methylbenzoyl chloride (20)(obtained according to procedures set forth in U.S. Patent Application Serial No. 08/708,411, filed September 5, 1995, which is specifically incorporated by reference herein) (2.4 g, 11.5 mmol) in THF (4 mL) was added. After 2 :hours 50% aqueous NaOH (4.1 g, 2.8 mL, 52.2 mmol) was added ~~nd the mixture was heated under reflux for 1 hour. After c~~oling to ambient temperature, the mixture was neutralized to pH = 7 with 2 N aqueous HC1 (26 mL).
This mixture was diluted with EtOAc (500 mL) and washed with H20 (1 x 250 mL) , satuo~ated aqueous NaHC03 (2 x 250 mL) , Hz0 (1 x 250 mL), and brine (1 x 125 mL). The organic layer was dried (Na~S09) and purified by flash chromatography {75/25 EtOAc/hexanes) to give amide 21 as a white foam {1173-57A, 1 . 3 9 g, 23 % ) . T:ze 1H t~TMR indicated the presence of 11 wt EtOAc which coul~3 not be removed in vacuo.
SUBSTITUTE SHEET (RULE 26) Analysis:
1H NMR (300 MHz, CD~OD) S 7.53 (d, J = 7.3 Hz, 2 H} , 7.32 (t, J = 7.0 Hz, 2 H), 7.20 (t, J = 7.3 Hz, 1 H}, 7.06 (t, J =
BACKGROUND AND SUMMAR~i' OF THE INVENTION
This invention relates to a novel series of chemical compounds useful as HI:V protease inhibitors and to the use of such compounds as antiviral agents.
Acquired Immune L>eficiency Syndrome (AIDS) is a rela-tively newly recognized disease or condition. AIDS causes a gradual breakdown of the body's immune system as well as progressive deterioration of the central and peripheral nervous systems. Since its initial recognition in the early 1980's, AIDS has spread rapidly and has now reached epidemic proportions within a relatively limited segment of the population. Intensive research has led to the discovery of the responsible agent, human T-lymphotropic retrovirus III
(HTLV-III), now more commonly referred to as the human immunodeficiency virus; or HIV.
HIV is a member c>f the class of viruses known as retroviruses. The ret.roviral genome is composed of RNA
which is converted to DNA by reverse transcription. This retroviral DNA is then stably integrated into a host cell's chromosome and, emplo~~ing the replicative processes of the host cells, produces new retroviral particles and advances the infection to other cells. HIV appears to have a particular affinity for the human T-4 lymphocyte cell which plays a vital role in the body's immune system. HIV
infection of these white blood cells depletes this white cell population. Eventually, the immune system is rendered inoperative and ineffective against various opportunistic diseases such as, among others, pneumocystic carini pneumonia, Kaposi's sarcoma, and cancer of the lymph system.
Although th.e exact mechanism of the formation and work-ing of the HIV virus i.s not understood, identification of the virus has le:d to some progress in controlling the disease. For example, the drug azidothymidine (AZT) has been found effective f:or inhibiting the reverse transcription of the retroviral genome of the HIV virus, SUBSTITUTE SHEET (RULE 26) thus giving a measure of control, though not a cure, for patients afflicted with AIDS. The search continues for drugs that can cure or at least provide an improved measure of control of the deadly HIV virus.
Retroviral replication routinely features post-translational processing of polyproteins. This processing is accomplished by virally encoded HIV protease enzyme.
This yields mature polypeptides that will subsequently aid in the formation and function of infectious virus. If this molecular processing is stifled, then the normal production of HIV is terminated. Therefore, inhibitors of HIV protease may function as anti-HIV viral agents.
HIV protease is one of the translated products from the HIV structural protein pol gene. This retroviral protease specifically cleaves other structural polypeptides at discrete sites to release these newly activated structural proteins and enzymes, thereby rendering the virion replication-competent. As such, inhibition of the HIV
protease by potent compounds may prevent proviral integration of infected T-lymphocytes during the early phase of the HIV-1 life cycle, as well as inhibit viral proteolytic processing during its late stage. Additionally, the protease inhibitors may have the advantages of being more readily available, longer lived in virus, and less toxic than currently available drugs, possibly due to their specificity for the retroviral protease.
In accordance with this invention, there is provided a novel class of chemical compounds that can inhibit and/or block the activity of the HIV protease, which halts the proliferation of HIV virus, pharmaceutical compositions containing these compounds, and the use of the compounds as inhibitors of the HIV protease.
The present invention relates to compounds falling within formula (9) below, and pharmaceutically acceptable salts, prodrugs, and solvates thereof, that inhibit the protease encoded by human immunodeficiency virus (HIV) type 1 (HIV-1) or type 2 (HIV-2). These compounds are useful in the treatment of infection by HIV and the treatment of the-SUBSTITUTE SHEET (RULE 26) acquired immune deficiency syndrome (AIDS). The compounds, their pharmaceutically acceptable salts, and the pharmaceutical compositions of the present invention can be used alone or in combination with other antivirals, immunomodulators, antibiotics or vaccines. Compounds of the present invention ca.n also be used as prodrugs. Methods of treating AIDS, methods of treating HIV infection and methods of inhibiting HIV protease are disclosed.
The compounds of the present invention are of the formula (9):
R
Me O SPh O~N=R' HO , _ H OH N H
H
wherein:
R and R' <~re independently selected from H, a substituted or unsubstituted alkyl-OR1 group, a cycloalkyl group substitui~ed with a (C,-C6) alkyl group or a (C1-C~)alkyl-OH group, a heterocycle group substituted with a (C1-C6) alkyl gr~~up or a (C,-C6) alkyl-OH group, an alkyl-NRzR3 group, or an a:Lkyl-S (X) (Y) R4 group, wherein R1 is H, a. substituted or unsubstituted alkyl group, or an acyl group;
RZ and R3 ;ire each independently selected from H, substituted or mnsubstituted alkyl, cycloalkyl, heterocyc_Le, and aryl groups, and acyl and sulfonyl groups;
Rq is H, a substituted or unsubstituted alkyl, cycloalky~_, het~=_rocycle, or aryl group; and X and Y are each independently selected from =O and nothing;
or a pharmaceut:icall~~ acceptable prodrug, salt or solvate thereof.
SUBSTITUTE SHEET (RULE 26) WO 98/40357 PCTlUS98/04735 Preferably in the compounds of formula 9, R is H. More preferably, R is H and R' is a cycloalkyl group selected f rom CHzOH CH3 CHzOH CHzOH
. and Preferably in the compounds of formula 9 when at least one of R and R' is an alkyl-OR1 group, R, is H. Particularly when at least one of R and R' is an alkyl-OR1 group, the alkyl-ORl is selected from -C (CH3) ZCHZOH, -CH (CH3) CHZOH, -CHzCHzOH, -C (CH3) (CHzOH) 2, -C (CH3) ?-O-CHI-O-CH3, -C (CHI) zCH2-O-CHZ-O-CH3, and -C (CH3) ZCH2-O-acyl, or a pharmaceutically acceptable prodrug, salt or solvate thereof.
Preferably when at least one of R and R' is a cycloalkyl group substituted with a (C,-C6)alkyl group or a (C1-C6)alkyl-OH group, the cycloalkyl group is selected from:
s CH3 ' CH3 _ CH2QH CH3 CHzOH CHzOH
. and Preferably when at least one of R and R' is a heterocycle group substituted with a (C1-C6) alkyl group or a (C1-C6)alkyl-OH group, the heterocycle group is selected from:
H3C H3C HaC C H3 'S
O° S' , S , N /
O ° ~ , C IN-R3> and wherein R3 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group, or an acyl or sulfonyl group.
A preferred species of the formula (9) is [3S-[2(2S*,3S*),3 alpha,4a beta,8a beta]]-N-(1,1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-SUBSTITUTE SHEET (RULE 26) methylbenzoyl)~~mino]-4-(phenylthio)butyl]-3-isoquinolineca:rboxamide H
Me O SPh O~N
~~ OH
H~~ ' Me Me y ~N wN
H ~ H
H
and its pharmaceutically acceptable salts, and its prodrug analogs. Preferred prodrugs can be obtained by replacing the hydrogen in one of the alcohol groups with an acyl group, and more preff~rably an amino acid acyl group.
The present invention further provides pharmaceutical formulations compris_Lng an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof, in combination with a pharmaceutically acceptable carrier, such as a dilue~nt or excipient.
The present invention further provides a method of treating AIDS compri:~ing administering to a host or patient, such as a primate, an effective amount of a compound of the present invention.
The present invention further provides a method of inhibiting HIV replication comprising administering to an HIV infected cell, a cell susceptible to HIV infection or a host or patient, such as a primate, an effective amount of a compound of the present invention.
Det;~iled Description of the Invention The present invE:ntion provides new compounds falling within formula (9), as described above, that are useful for treating HIV infection and/or AIDS.
Applicants incorporate by reference U.S. Patent No.
5,484,926, U.S. Patent Application Nos. 08/708,411 and 08/708,607, and Japanese Patent Application Nos. JP 95-2481.83 and JP 95-2481.84, with the caveat that the definitions of preferences, terms, variables, labels and the SUBSTITUTE SHEET (RULE 26) like used in each application are applicable only to the corresponding disclosure from that application.
In particular, since each of the above-identified applications incorporated by reference was prepared separately, the original applications may use in some instances the same term, label or variable to mean something different. For example, the variable "X" is used in each application, but each application has its own distinct definition of the substituent or moiety represented by this variable. It will be apparent to those skilled in the art that the terms, labels and variables in each application incorporated by reference are limited solely to the disclosure from that application, and may be replaced by other suitable terms, labels and variables or the like representing the particular substituents and moieties. Of course, those skilled in the art will realize that any suitable set of terms, labels and variables may be used to generically or more specifically represent the subject matter disclosed in the present application, including terms, labels, variables, and the like universally applicable to the incorporated disclosures of the above-identified applications and the following disclosure.
Compounds of the formula (9) may be prodrugs, which can serve to improve the pharmaceutical properties of the compounds, such as pharmacokinetic properties, for example, improved bioavailability or solubility. The preparation of prodrugs may be carried out by standard methods known to those skilled in the art. A preferred prodrug can be obtained by acylation or alkylation of the starting alcohol when R or R' is CH ( CH3 ) ZCHZOH .
All temperatures stated herein are in degrees Celsius (°C). All units of measurement employed herein are in weight units except for liquids which are in volume units.
The term "alkyl" as used herein refers to straight or branched chain groups, preferably, having one to eight, more preferably having one to six, and most preferably having from one to four carbon atoms. The term "C1-C6 alkyl"
represents a straight or branched alkyl chain having from.
SUBSTITUTE SHEET (RULE 26) one to six carbon atoms. Exemplary C1-C6 alkyl groups include methyl,, ethyl, n- propyl, isopropyl, butyl, isobutyl, sec-butyl, t-butyl, pentyl, neo-pentyl, hexyl, isohexyl, and t:he like. The term "C1-C6 alkyl" includes within its def_Lnition the term "C1-CQ alkyl" .
The term "cyclo<~lky1" represents a saturated or partially saturated, mono- or poly-carbocylic ring, preferably having 5-:14 ring carbon atoms. Exemplary cycloalkyls include monocyclic rings having from 3-7, preferably 3-6, carbon atoms, such as cyclopropyl, cyclobutyl, cyc:lopent:yl, cyclohexyl, cycloheptyl and the like. An exemplary cycloalkyl is a C,-C~ cycloalkyl, which is a saturated hydrocarbon ring structure containing from five to seven carbon atoms.
The term "alkoxyl" represents -O-alkyl. An example of an alkoxyl is a C1-C6 alkoxyl, which represents a straight or branched alkyl chain having from one to six carbon atoms attached to an oxygen atom. Exemplary C1-C~ alkoxyl groups include methox:yl, et:hoxyl, propoxyl, isopropoxyl, butoxyl, sec-butoxyl, t-butoxyl, pentoxyl, hexoxyl, and the like.
C1-C6 alkoxyl include; within its definition a C1-Cq alkoxyl.
The term "aryl" as used herein refers to a carbocyclic or heterocyclic, aromatic, 5-14 membered monocyclic or polycyclic ring. Exemplary aryls include phenyl, naphthyl, anthryl, phenan.thryl, thienyl, pyrrolyl, imidazolyl, pyrazolyl, furyl, isothiazolyl, furazanyl, isoxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, benzo[b]thienyl, naphtho[2,3-b]thianthrenyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxathienyl, indolizinyl, isoindolyl, indolyl, indazolyl, purinyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl, quinoxyalinyl, quinzolinyl, benzothiazolyl, benzimidazolyl, tetrahydroquinolinyl, cinnolinyl, pteridinyl, carbazolyl,~
beta-carbolinyl, phenanthridinyl, acridinyl, perimidinyl, phenanthrolinyl, phen.azinyl, isothiazolyl, phenothiazinyl, and phenoxazinyl.
The term "arylox.yl" represents -O-aryl.
SUBSTITUTE SHEET (RULE 26) _g_ The term "hydrolyzable group" is a group, which when bonded to an oxygen, forms an ester, which can be hydrolyzed in vivo to a hydroxyl group. Exemplary hydrolyzable groups, which are optionally substituted, include acyl function, sulfonate function and phosphate function. For example, such hydrolyzable groups include blocked or unblocked amino acid residue, a hemisuccinate residue, and a nicotinate residue.
The term "halogen" represents chlorine, fluorine, bromine or iodine. The term "halo" represents chloro, fluoro, bromo or iodo.
The term "carbocycle" represents an aromatic or a saturated or a partially saturated 5-14 membered monocyclic or polycyclic ring, such as a S- to 7-membered monocyclic or 7- to 10-membered bicyclic ring, wherein all the ring members are carbon atoms.
The term "heterocycle" represents an aromatic or a saturated or a partially saturated, 5-14 membered, monocylic or polycyclic ring, such as a 5- to 7-membered monocyclic or 7- to 10-membered bicyclic ring, having from one to three heteroatoms selected from nitrogen, oxygen and sulfur, and wherein any nitrogen and sulfur heteroatoms may optionally be oxidized, and any nitrogen heteroatom may optionally be quaternized. The heterocyclic ring may be attached at any suitable heteroatom or carbon atom. Examples of such heterocycles include decahydroisoquinolinyl, octahydro-thieno[3,2-c]pyridinyl, piperidinyl, piperazinyl, azepinyl, pyrrolyl, pyrrolidinyl, pyrazolyl, pyrazolidinyl, imidazolyl, isobenzofuranyl, furazanyl, imidazolinyl, imidazolidinyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, oxazolyl, oxazolidinyl, isoxazolyl, thianthrenyl, triazinyl, isoxazolidinyl, morpholinyl, thiazolyl, thiazolidinyl, isothiazolyl, quinuclidinyl, iso-thiazolidinyl, indolyl, quinolinyl, chromenyl, xanthenyl, isoquinolinyl, benzimidazolyl, thiadiazolyl, benzopyranyl, benzothiazolyl, benzoazolyl, furyl, tetrahydrofuryl, tetrahydropyranyl, thienyl, benzothienyl, benzo[b]thienyl, naphtho[2,3-b]thienyl, thiamorpholinyl, SUBSTITUTE SHEET (RULE 26) thiamorpholiny:Lsulfoxide, thiamorpholinylsulfone, oxadiazolyl, t:riazolyl, tetrahydroquinolinyl, tetrahydriso-quinolinyl, phc~noxathienyl, indolizinyl, isoindolyl, indazolyl, pur:inyl, isoquinolyl, quinolyl, phthalazinyl, naphthyridinyl,, quinoxyalinyl, quinzolinyl, tetrahydroquinolinyl, cinnolinyl, pteridinyl, carbazolyl, beta-carboliny=L, phenanthridinyl, acridinyl, perimidinyl, phenanthroliny=L, phenazinyl, isothiazolyl, phenothiazinyl, and phenoxazinyl.
The term "thioether" includes S-aryl, such as phenylthio and naphtlzylthio; S-heterocycle where the heterocycle is saturated or partially saturated;
S- (CS-C~) -cycloalkyl; and S-alkyl, such as C,-C~ alkylthio.
In the thioether, the=_ -aryl, the -heterocycle, the -cycloalkyl anc~ the --alkyl can optionally be substituted.
An example of a thioether is "C1-C6 alkylthio", which represents a st;raight~ or branched alkyl chain having from one to six carbon atoms attached to a sulfur atom.
Exemplary Cl-C6 alkylthio groups include methylthio, ethylthio, propylthio, isopropylthio, butylthio, sec-butylthio, t-bL~tylth_Lo, pentylthio, hexylthio, and the like.
The term "mercapto" represents -SH.
The term "amino" represents -NL1L2, wherein Ll and LZ
are preferably indepE:ndently selected from oxygen, carbocycle, het.erocyc:le, alkyl, sulfonyl and hydrogen; or NC (0) L3, wherein L3 is preferably alkyl, alkoxyl, hydrogen or -NL~L~. The ar~~l, alltyl and alkoxyl groups can optionally be substituted. A,n example of an amino is C1-C9 alkylamino, which represents a straight or branched alkyl chain having from one to four carbon atoms attached to an amino group.
Exemplary C1-C9 alkylamino groups include methylamino, ethylamino, propylam.i_no, isopropylamino, butylamino, sec-butylamino, and. the 7.ike. Another example of an amino is di(C1-C9)alkylamino, which represents two straight or branched alkyl chain~~, each having from one to four carbon atoms attached to a common amino group. Exemplary di(C1-CQ)alkylamino groups include dimethylamino, ethylmethylamino, met:hylpropylamino, ethylisopropylamino, SUBSTITUTE SHEET (RULE 26) butylmethylamino, sec-butylethylamino, and the like. An example of an amino is C1-Cq alkylsulfonylamino, which has a straight or branched alkyl chain having from one to four carbon atoms attached to a sulfonylamino moiety. Exemplary C1-Cq alkylsulfonylamino groups include methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, isopropylsulfonylamino, butylsulfonylamino, sec-butylsulfonylamino, t-butylsulfonylamino, and the like.
The term "acyl" represents L6C(O)L4, wherein L6 is a single bond, -O or -N, and further wherein Lq is preferably alkyl, amino, hydroxyl, alkoxyl or hydrogen. The alkyl and alkoxyl groups can optionally be substituted. An exemplary acyl is a C1-C~ alkoxycarbonyl, which is a straight or branched alkoxyl chain having from one to four carbon atoms attached to a carbonyl moiety. Exemplary C,-CQ
alkoxycarbonyl groups include methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, and the like. Another exemplary acyl is a carboxy wherein L6 is a single bond and Lq is alkoxyl, hydrogen, or hydroxyl. A further exemplary acyl is N-(C1-C9) alkylcarbamoyl (L6 is a single bond and L4 is an amino) , which is a straight or branched alkyl chain having from one to four carbon atoms attached to the nitrogen atom of a carbamoyl moiety. Exemplary N-(C1-Cq)alkylcarbamoyl groups include N-methylcarbamoyl, N-ethylcarbamoyl, N-propylcarbamoyl, N-isopropylcarbamoyl, N-butylcarbamoyl, and N-t-butylcarbamoyl, and the like. Yet another exemplary acyl is N,N-di(C1-C4)alkylcarbamoyl, which has two straight or branched alkyl chains, each having from one to four carbon atoms attached to the nitrogen atom of a carbamoyl moiety. Exemplary N,N-di(C1-C4)alkylcarbamoyl groups include N,N-dimethylcarbamoyl, N,N-ethylmethylcarbamoyl, N,N-methylpropylcarbamoyl, N,N-ethylisopropylcarbamoyl, N,N-butylmethylcarbamoyl, N,N-sec-butylethylcarbamoyl, and the like.
The term "sulfinyl" represents -SO-L5, wherein LS is preferably alkyl, amino, aryl, cycloalkyl or heterocycle.
SUBSTITUTE SHEET (RULE 26) The alkyl, aryl, cycloalkyl and heterocycle can all optionally be substituted.
The term "sulfonyl" represents -SOz-L5, wherein LS is preferably alkyl, aryl, cycloalkyl, heterocycle or amino.
The alkyl, aryl, cycloalkyl and heterocycle can all optionally be substituted. An example of a sulfonyl is a C1-Cq alkylsulfonyl, which is a straight or branched alkyl chain having from one to four carbon atoms attached to a sulfonyl moiety. Exemplary C1-Cq alkylsulfonyl groups include methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfo:zyl, butylsulfonyl, sec-butylsulfonyl, t-butylsulfonyl ;end the like.
As indical~ed above, many of the groups are optionally substituted. :Ln fact, unless specifically noted, all of the groups defined by the terms defined in this application may be substituted or unsubstituted. For instance, when the term "alkyl" i:~ used, it should be understood to encompass both substituted and unsubstituted alkyl unless specific exclusion of one or the other is positively stated.
Examples of substituents for alkyl and aryl include mercapto, thioether, nitro (NOZ), amino, aryloxyl, halogen, hydroxyl, alko~tyl, and acyl, as well as aryl, cycloalkyl and saturated and partially saturated heterocycles. Examples of substituents for hetE~rocycle and cycloalkyl include those listed above for alkyl and aryl, as well as aryl and alkyl.
Exemplary substituted aryls include a phenyl or naphthyl ring :~ubstii:uted with one or more substituents, preferably one to three substituents, independently selected from halo, hydx-oxy, rnorpholino (C1-CQ) alkoxy carbonyl, pyridyl (C1-C~) alkoxycarbonyl, halo (C1-Cq) alkyl, C1-C9 alkyl, C1-C9 alkoxy, carbox~~, C1-C'q alkoxycarbonyl, carbamoyl, N- (Ci-C9) alkylcarbamo:yl, amino, C1-Cq alkylamino, di (C1-CQ) alkyl amino o:r a group of the formula -(CH2)a-R~ where a is 1, 2, 3 or 4; and ~.~ is hydroxy, C1-C~
alkoxy, carboxy, C1-Cq alkoxycarbonyl., amino, carbamoyl, C1-C9 alkyl amino or d:i (C1-C9) alkyl amino.
Another substituted alkyl is halo(C,-Cq)alkyl, which represents a straight: or branched alkyl chain having from-SUBSTITUTE SHEET (RULE 26) one to four carbon atoms with 1-3 halogen atoms attached to it. Exemplary halo(C1-C9)alkyl groups include chloromethyl, 2- bromoethyl, 1-chloroisopropyl, 3-fluoropropyl, 2,3-dibromobutyl, 3-chloroisobutyl, iodo-t-butyl, trifluoromethyl and the like.
Another substituted alkyl is hydroxy(C1-CQ)alkyl, which represents a straight or branched alkyl chain having from one to four carbon atoms with a hydroxy group attached to it. Exemplary hydroxy(C1-CQ)alkyl groups include hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, 2-hydroxy-isopropyl, 4-hydroxybutyl and the like.
Yet another substituted alkyl is C1-C9 alkylthio(C;-C4) alkyl, which is a straight or branched Cl-C9 alkyl group with a C1-CG alkylthio group attached to it. Exemplary C1-C, alkylthio(C1-Cq)alkyl groups include methylthiomethyl, ethylthiomethyl, propylthiopropyl, sec-butylthiomethyl, and the like.
Yet another exemplary substituted alkyl is heterocycle(C1- C9)alkyl, which is a straight or branched alkyl chain having from one to four carbon atoms with a heterocycle attached to it. Exemplary heterocycle(C1-CQ)alkyls include pyrrolylmethyl, quinolinyl-methyl, 1-indolylethyl, 2-furylethyl, 3-thien-2-ylpropyl, 1-imidazolylisopropyl, 4-thiazolylbutyl and the like.
Yet another substituted alkyl is aryl(C1-Cq)alkyl, which is a straight or branched alkyl chain having from one to four carbon atoms with an aryl group attached to it.
Exemplary aryl(Cl-C9)alkyl groups include phenylmethyl, 2-phenylethyl, 3-naphthyl-propyl, 1-naphthylisopropyl, 4-phenylbutyl and the like.
The heterocycle can, for example, be substituted with 1, 2 or 3 substituents independently selected from halo, halo (C~- CQ ) alkyl , C,-Cq alkyl , C1-C4 alkoxy, carboxy, CI-C9 alkoxycarbonyl, carbamoyl, N-(C,-CQ)alkylcarbamoyl, amino, C1-CQalkylamino, di (C1-CQ) alkyl amino or a group having the structure - (CHZ) a-R' where a is 1, 2, 3 or 4 and R' is hydroxy, C2-CQ alkoxy, carboxy, C1-Cq alkoxycarbonyl, amino, carbamoyl, C1-Cq alkyl amino or di (C,-C4) alkylamino.
SUBSTITUTE SHEET (RULE 26) Examples of substituted heterocycles include 3-N-t-butyl carboxam.ide decahydroisoquinolinyl, 6-N-t-butyl carboxamide octahydro-thieno[3,2-c]pyridinyl, 3-methylimidazolyl, 3-methoxypyridyl, 4-chloroquinolinyl, 4-aminothiazolyl, 8-methylquinolinyl, 6-chloroquinoxalinyl, 3-ethylpyridyl, 6-methoxybenzimidazolyl, 4-hydroxyfuryl, 4-methylisoqui:aolinyl, 6,8-dibromoquinolinyl, 2-methyl-1,2,3,4-tetrahydroisoquinolinyl, N-methyl-quinolin-2-yl, 2-t-butoxycarbc~nyl-1,2,3,4-isoquinolin-7-yl and the like.
Exemplary heterocyclic ring systems represented by A or B include (1) !~-membered monocyclic ring groups such as thienyl, pyrro:lyl, ivmidazolyl, pyrazolyl, furyl, isothiazolyl, :Euraza:nyl, isoxazolyl, thiazolyl and the like;
(2) 6-membered monocyclic groups such as pyridyl, pyrazinyl, pyrimidinyl, p~~ridazinly, triazinyl and the like; and (3) polycyclic hete~rocyc:lic rings groups, such as decahydroisoquinolinyl, octahydro-thieno [3,2-c] pyridinyl, benzo [b] thieny:L , naphtho [2 , 3 -b] thianthrenyl , isobenzofurany:L,_chromenyl, xanthenyl, and fully or partially saturated analogs thereof.
A cycloallcyl ma~~ be optionally substituted with 1, 2 or 3 substituents indepE=_ndently selected from halo, halo (C~-C~) alky:L, C1-C9 alkyl, C1-Cq alkoxy, carboxy, C1-C4 alkoxycarbonyl , carbamoyl , N- ( C, -CQ ) alkyl carbamoyl , amino , Cl-Cq alkyl amino, di (Ci-C~) alkylamino or a group having the structure - (CH2) a-R' where a is 1, 2, 3 or 4 and R' is hydroxy, Cl-C9 alkoxy, carboxy, C1-Cq alkoxycarbonyl, amino, carbamoyl, Cz-C9 alkylamino or di (C,-C9) alkyl amino.
Exemplary substituted cycloalkyl groups include 3-methylcyclopE:ntyl, 4-ethoxycyclohexyl, 5-carboxycyclo-~hepty:L, 6-chlorocyclohexyl and the like.
Exemplary substituted hydrolyzable groups include N-benzyl glycyl., N-Cbz-L-valyl, and N-methyl nicotinate.
The compounds of the present invention have at least five asymmetric: centers denoted by an asterisk in the formula (9) below:
SUBSTITUTE SHEET (RULE 26) SPh Me O Oa-N:R
HO N** N
H OH H
H
As a consequence of these asymmetric centers, the compounds of the present invention can occur in any of the possible stereoisomeric forms, and can be used in mixtures of stereoisomers, which can be optically active or racemic, or can be used alone as essentially pure stereisomers, i.e., at least 95% pure. All asymmetric forms, individual stereoisomers and combinations thereof, are within the scope of the present invention.
The individual stereoisomers may be prepared from their respective precursors by the procedures described above, by resolving the racemic mixtures, or by separating the diastereomers. The resolution can be carried out in the presence of a resolving agent, by chromatography or by repeated crystallization or by some combination of these techniques which are known in the art. Further details regarding resolutions can be found in Jacques et al., Enantiomers, Racemates, and Resolutions, John Wiley & Sons 1981.
Preferably, the compounds of the present invention are substantially pure, i.e, over 50o pure. More preferably, the compounds are at least 75% pure. Even more preferably, the compounds are more than 90% pure. Even more preferably, the compounds are at least 95% pure, more preferably, at least 97o pure, and most preferably at least 99o pure.
As mentioned above, the invention includes the pharmaceutically acceptable salts of the compounds defined by formula (9). A compound of this invention may possess a sufficiently acidic, a sufficiently basic, or both functional groups, and accordingly react with any of a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.
SUBSTITUTE SHEET (RULE 26) The term "pharmaceutically acceptable salt", as used herein, refers to salts of the compounds of the above formula which ;ire substantially non-toxic to living organisms. Exemplary pharmaceutically acceptable salts include those ;alts prepared by reaction of the compounds of the present im;rention with a mineral or organic acid or an inorganic base. The reactants are generally combined in a mutual solvent such .as diethylether or benzene, for acid addition salts,, or water or alcohols for base addition salts. The sa_Lts normally precipitate out of solution within about one hour to about ten days and can be isolated by filtration or other conventional methods. Such salts are known as acid addition and base addition salts.
Acids that: may be employed to form acid addition salts are inorganic ciCldS such as hydrochloric acid, hydrobromic acid, hydroiod~_c acid, sulfuric acid, phosphoric acid, and the like, and organic acids such as p-toluenesulfonic, methanesulfonic: acid,, oxalic acid, p-bromophenylsulfonic acid, carbonic acid, succinic acid, citric acid, benzoic acid, acetic acid, and the like.
Examples of pharmaceutically acceptable salts are the sulfate, pyrosulfate, bisulfate, sulfite, bisulfate, phosphate, monohydroc~enphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate, propionate, decanoate, caprylate, acrylate, formate, isobutyrate, caproate, heptanoate, propiolate, oxalate, malona.te, succinate, suberate, sebacate, fumarate, maleate, butyne-1,4-c~ioate, hexyne-1,6-dioate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, hydroxybenzoate, methoxybenzoate, phthalate, sulfonate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutyrate, citrate, lactate, g-hydroxybutyrate, glycollate, tartrate, methane-sulfonate, propanesulfonate, naphthalene-1-sulfonate, napththalene-2-sulfonate, mandelate and the like.
Preferred pharmaceutically acceptable acid addition salts are those formed with mineral acids such as hydrochloric acid anal hydrobromic acid, and those formed SUBSTITUTE SHEET (RULE 26) with organic acids such as malefic acid and methanesulfonic acid.
Base addition salts include those derived from inorganic and organic bases, such as ammonium or alkali or alkaline earth metal hydroxides, carbonates, bicarbonates, and the like. Such bases useful in preparing the salts of this invention thus include sodium hydroxide, potassium hydroxide, ammonium hydroxide, potassium carbonate, sodium carbonate, sodium bicarbonate, potassium bicarbonate, calcium hydroxide, calcium carbonate and the like. The potassium and sodium salt forms are particularly preferred.
A "pharmaceutically acceptable prodrug" is intended to mean a compound that may be converted under physiological conditions or by solvolysis to a compound of the formula 9.
A "pharmaceutically acceptable solvate" is intended to mean a solvate that retains the biological effectiveness and properties of the biologically active components of compounds of formula 9.
Examples of pharmaceutically acceptable solvates include, but are not limited to, compounds of formula 9 in combing ion with water, isopropanol~, ethanol, methanol, DMSO, ethyl acetate, acetic acid, or ethanolamine.
It should be recognized that the particular counterion forming a part of any salt of this invention is not of a critical nature, so long as the salt as a whole is pharmacologically acceptable and as long as the counterion does not contribute undesired qualities to the salt as a whole.
SUBSTITUTE SHEET (RULE 26) A preferred compound is compound 21 H
Me O sPh O~N
~~ OH
HO - Me Me 1 \ ~N N
lI H OH H
H
[3S- [2 (2S*, 3S* ) , 3 alpha, 4a beta, 8a beta] ] -N- (1, 1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino)-4-(phenylthio)butyl]-3-isoquinolinecarboxamide.
A process for making compound 21 is provided below.
Compound 21 ha:~ also been obtained as a metabolite from the plasma of patients administered [3S-(3R,4aR*,8aR*,a?'S*,3'S*)]-2-[2'-hydroxy-3'-phenylthiomethyl-4' -aza-5' -oxo-Vii' - (2 " -methyl-3 "-hydroxyphenyl) pentyl]
decahydroisoquinolinc=_-3-N-t-butylcarboxamide methanesulfonic acid salt, which is disclosed in U.S. Patent No. 5,484,926.
The compounds o:E formula 9 can be prepared according to the following F:eaction Scheme I.
SUBSTITUTE SHEET (RULE 26) REACTION SCHEME I
Scheme I. General Synthetic Pathway for the Production of 96 and Derivatives R
CONHt-Bu OOOH COOH R R~ Oy N' R' aqums H' N H Mdto~s H' N H Ami~ePrdedon ~~ N . H ' H Rp~ N
--w ----s H
H Step la H Step Ib H
Artidecwpiog H
Step 1 to 2a 2b Rp =artcx prteauggoup 3 SPh R
CbzHN~CI R R
O~N R SPh O tV SPh O~N,R, H.N OH 5 ~_ 'R~ Chrrertnval H CHotoarohol qty N ~ H_N~N
L~proteaon ~ OFI H OH ~H
H epoxide Step xI~lIS
Step 3 cbse-open seqmrce H H
q 6 Step 4 Me AcO~COQ R R
Me p SPh O~ N, R, Me O SPh O~ N, R
acetate g Ac0 ~ ~' mmval NFI Y 'N HO ~ ~
H NH Y 'N
antis coplo~ OH ~ OH H
Step 6a H~ ~eP 66 9a H
9b Compound 1a, perhydroisoquinoline, which is commercially available from NSC Technologies (Chicago, IL) or Procos SpA (Milan, Italy) is subjected to prolonged acid hydrolysis in step 1a to obtain compound 2a. A variety of inorganic acids may be used in either an aqueous/organic solvent mixture or in water alone at temperatures above 50 °C. An example of such an inorganic acid is 6N aqueous HCl.
Substitutes for compound la include the corresponding esters lb, thioesters lc or other amides ld:
H COOZ H COSZ CONZ~ZZ
H
H H
H
H ~ ~ H
lb lc ld , where Z, Z1 and Zz may each independently be alkyl, cycloalkyl, heterocycle, or aryl.
SUBSTITUTE SHEET (RULE 26) Compound 2~~ is then protected at the amine nitrogen to obtain compound 2b in step Ib. The protecting group Rp is defined as a suitably conjugating group to avoid unwanted decomposition oi= activated carboxylate derivatives of compound 2b in ~>tep 2. Such protecting groups typically can be carbamate in origin, having a general structure of formula 11:
O
R"O~
The identity of R" in formula 11 can be any alkyl, cycloalkyl, aryl, or heterocycle which can be removed easily in a deprotection step after Step,2. Examples of R"
include, but are not limited to methyl, ethyl, propyl, isopropyl, n-butyl, i:~obutyl, t-butyl or higher branched or unbranched alkyl, 2,2,2-trichloroethyl, 2-trimethylsilylethyl, allyl, phenyl, substituted phenyl, benzyl, substituted benzyl, 9-fluorenylmethyl, 9-anthrylmethyl anal higher polycyclic aromatic ring system.
The following materials, as defined below, can be obtained from the Aldrich Chemical Co. (Sigma Aldrich Fluka):
a 2.2,2-trichloroethyl= -a-12-C-a a H a~3 2-trimethylsllylethyl= -~2-C-SI--a'13 H a-13 allyl= -a-IZ-CH=Cii2 henzyl= _ q.~ / \
9-flourenylmethyl =
I
9-anihrylnethyt =
SUBSTITUTE SHEET (RULE 26) Such protecting groups typically can be installed by an acylation reaction of the corresponding haloformate ester 12a or a dicarbonate 12b:
O O
I~'O~X R"O~Y
12a 12b X = halogen Y = OCOR"
in the presence of a suitable base in typical organic solvents for these types of reactions such as halogenated solvents, ethers and hydrocarbons. Such bases are typically inorganic, such as metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, 1,8-diazabicyclo[2.2.2)octane (DABCO) or related di- or trialkyl-amines, as well as amidine bases like 1,8-diazabicyclo [5.4 . 0) under-7-ene (DBU) and 1, 8-diazabicyclo[4.3.0]non-5-ene (DBN). The following materials, as defined below, can be obtained from the Aldrich Chemical Co. (Sigma Aldrich Fluka):
~aaoo =
oBU = ~~
These reactions are typically run anywhere from below room temperature to approximately 100 °C.
The amide coupling Step 2 can be accomplished in any number of fashions depending on how the carboxyl group is activated. A group J is installed in Step 2 by reaction of the carboxylic acid 2b to produce the activated derivative 2c.
SUBSTITUTE SHEET {RULE 26) Sten 2 J R
COOH 05! I
activaW nofthe Rpm R~N~R O~ N~R
N H carboxyl goup N H H ~~ N
-----~ H
H H ~ base H
2b Rp = am~e protect~g goy 2c J = leav~g goup 3 The group ~T can be any of a variety of leaving groups such as alkoxy, hydroxy, halogen, pseudohalogen (including azide, cyanide, isocy<~nate and isothiocyanate), alkyl or arenesulfonate, aromatic heterocycle(bonded through a heteroatom) and N-hyd:roxyheterocycle, including hydroxysuccinimide or hydroxybenzotriazole ester. The following definitions apply to the terms above:
azide -N-t~N
cyanide -C=N
isocyanate-N=C=O
isothiocyanate-t~~g O
alkylsulfonate-O-S-alkyl i O
O
ii arenesuNonate-O-S-aryl O
N-hydroxyhe:erocyclic HO-where N~ = nitrogen heterocycle \~/O\\
N-hydroxysuccinimide HO-N
O
hyd roxybe nnotriazo le ~I N
N
OH
SUBSTITUTE SHEET (RULE 26) The aryl halides (2c, J = halogen) may be prepared using inorganic halogenating agents such as thionyl chloride or bromide, phosphorous trichloride or bromide, phosphorous pentachloride or bromide or organic agents such as oxalyl chloride or trichlorisocyanuric acid. Esters (2c, J = OR") (R" is defined above) may be prepared in a variety of ways starting from the acid chloride 2c where J is Cl by combination with the desired alcohol in the presence of an organic or inorganic base stated previously for the acylation of compound 12a or compound 12b. Alternatively, the ester may be produced by acid-promoted esterification in the presence of the desired alcohol. The sulfonates (2c, J =
OSO~Wl, where Wl is alkyl or aryl) are typically made by reaction of the carboxylic acid 2b with alkyl or arylsulfonyl chlorides in the presence of an organic amine base such as triethylamine in a non-polar solvent at temperatures below 0 °C. Alkyl and arylsulfonyl are defined as follows:
alkylx~lfonylchloride = d-S-alkyl O
O
arenesulfonyl chloride = d-S-aryl O
The pseudohalogen derivatives of 2c (J = pseudohalogen) are typically made from the acid halides 2c (J = halogen) by reaction with inorganic pseudohalide in the presence of a base. Such bases include, but are not limited to metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, 1,8-diazabicyclo[2.2.2]octane (DABCO) or related di- or trialkylamines, as well as amidine bases like 1,8-diazabicyclo[5.4.0]under-7-ene (DBU) and 1,8-diazabicyclo[4.3.0]non-5-ene (DBN). A particularly preferred base is triethylamine. The heteroaromatic SUBSTITUTE SHEET (RULE 26) derivatives of 2c are also made from the acid halides 2c (J
- halogen), utilizing the specific heteroaromatic compound in the presence of an amine base in a non-polar solvent.
The N-hydroxyher_erocyclic derivatives of 2c can be made from the acid halide; as above and may also be generated using alkyl carbodiim:ides (.alkyl-N=C=N-alkyl, where the alkyl groups can be the same or different) or aryl carbodiimides (aryl-N=C=N-ary:L, where the aryl groups can be the same or different) and an amine base as condensing agents.
The primar~r or secondary amine (shown above the arrow in Step 2 of Scheme I,? used in the coupling process may incorporate suitable protecting groups, depending on the functionality present in the amine and the mode of coupling used. The mode of coupling of 2c with a primary or secondary amine can bE=_ carried out in a variety of ways depending on the' ident=ity of J. 4~Then a free acid is used (2c, J = OH) the. coupling can be performed using carbodiimide-ba~~ed methods utilizing any of the common reagents of thi:~ clas:~, including dicyclohexylcarbodiimide or related dialk:ylcarbodiimides, EDC (salts of 1- (3-dimethylaminopropyl)-.3-ethylcarbodiimide) or related water-soluble reagent; along with an organic amine base in polar organic solvent; such as dioxane, DMF, NMP and acetonitrile in the presence of an N-hydroxyheterocyclic compound such as N-hydroxysuccini.mide or 3-hydroxybenzotriazole.
Alternatively, halofox°mate esters, such as 12d, may be used to temporarily a.ctivat:e the acid to give mixed anhydrides of general formula 2d.
O~OR"
O:yO
R~~N- O
H
R"O~ X
H' 12d X = halogen 2d SUBSTITUTE SHEET (RULE 26) Such haloformate esters are typically as shown in 12d above and include methyl-, ethyl-, isopropyl-, isobutyl-, n-butyl, phenyl- and related alkyl and aryl chloroformates, defined below.
alkyl chloiofortnate = 'I
alkyl-O~Q
O
aryl chlorofortnate = aryl-O~C!
Formula 2d is a possible intermediate in the step from formula 2b to formula 3. Formula 2d is an intermediate, but the process described here results in formula 3, without isolation of Formula 2d.
These reactions are typically performed in a variety of non-polar organic solvents like halocarbons and ethers such as diethyl ether, methyl t-butylether, diisopropyl ether, dioxane and THF at temperatures below 0 °C accompanied by an organic amine base such as triethylamine, diethylamine, diethyl isopropylamine, DABCO or related di- or trialkylamines, as well as amidine bases like DBU and DBN.
When J in compound 2c is an alkyl or arenesulfonate (J
- OSOZR or OSO2Ar), the coupling can be performed in a variety of non-polar organic solvents like halocarbons and ethers, such as diethyl ether, methyl t-butylether, diisopropyl ether, dioxane and THF at temperatures below 0 °C, accompanied by an organic amine base such as triethylamine, diethylamine, diethyl isopropylamine, DABCO
or related di- or trialkylamines, as well as amidine bases like DBU and DBN.
When J in compound 2c is a halogen or pseudohalogen, the coupling may be performed in most common organic solvents such as THF, diethyl ether, dioxane, methyl t-butyl ether or other ethers; acetone, cyclohexanone, methyl isobutylketone and other ketones; esters such as ethyl, SUBSTITUTE SHEET (RULE 26) methyl and isopropyl acetate; halogenated solvents such as halogenated metlzanes and ethanes, chlorobenzene and other halogenated ben:~enes; nitrites such acetonitrile and propionitrile; :Lower alcohols such as ethanol, isopropanol, t-butanol and related alcohols; and polar organic solvents such as dimethy:Lformamide, dimethylsulfoxide, N-methyl-2-pyrrollidone and related amide-containing solvents. A base is frequently used and may be any of a number of inorganic bases such as metal hydroxides, bicarbonates and carbonates or organic baser such as amines like triethylamine, diethylamine, d~_ethyl isopropylamine, DABCO or related di-or trialkylamines, as well as amidine bases like DBU and DBN.
One skillecL in the art will be able to perform the amide coupling ~~tep 2 with other possible J groups.
In Step 3 protect=ing group removal can be accomplished using any of the standard methods for deprotecting a particular clas:~ of protecting group. Simple alkyl- and substituted alk~.Tl~carbamates can be removed with aqueous solutions of ba:>e at t=emperatures up to about 100 °C, employing any of: the common inorganic metal hydroxides such as sodium-, litriium-, potassium- or barium hydroxide or hydroxides of other metals in at least stoichiometric amounts. Carbamate protecting groups that contain benzyl groups bonded tc> oxygen may be removed by hydrogenolysis with a palladium or platinum catalyst. Alternatively, aqueous base hycLrolysis may be used at temperatures up to about 100 °C, employing any of the common inorganic metal hydroxides such as sodium-, lithium-, potassium- or barium hydroxide or hydroxides of other metals in at least stoichiometric a.mount~~. A variety of anhydrous acids may also be used for deprotection of benzyl-based carbamates, including HCl, H:Br and HI. Lewis acids of boron and aluminum such as A1C13, BBr3, BClj in non-polar solvents are also effective. Certain substituted benzyl, aryl or alkyl groups in which the specific substitution pattern is chosen for its ability to be removed under specific conditions may also be used. F'or example, the 2-SUBSTITUTE SHEET {RULE 26) trimethylsilylethylcarbonyl group (Teoc) is a protecting group designed to take advantage of the specific reactivity of the 2-trimethylsilylethyl group in the deprotection process. 2-Trimethylsilylethylcarbonyl chloride may be used to protect the amine nitrogen and may later be removed using sources of fluoride ion such as HF or tetraalkylammonium fluoride salts.
In Step 4, the perhydroisoquinoline piece of formula 4 is connected to the Chloroalcohol (compound 5, Scheme I) via an epoxide intermediate (13) generated via the base-induced closure of the vicinal chlorohydrin functionality.
SPh CbzHN
O
Compound 5 is produced by Kaneka Industries, Japan. Several close-open procedures in proceeding from compound 5 compound 13 ~ compound 6 may be used. The epoxide 13 may be isolated or it may be reacted with 4 added either subsequent to formation of 13 or 4 may be present from the beginning of the sequence. The epoxide 13 can be generated using inorganic bases such as metal hydroxides, carbonates and bicarbonates in solvents such as alcohols like methanol ethanol or isopropyl alcohol, ethers such as THF and dioxane or mixtures of the two. The epoxide can also be generated in a 2-phase solvent system consisting of water and a halocarbon solvent such as dichloromethane along with the base. A phase-transfer catalyst such as a tetraalkylammonium salt may be used to facilitate the process. The process of opening the epoxide 13 with compound 4 is accomplished in alcohol solvents or mixtures of an alcohol and another solvent which may be an ether or a Bipolar aprotic solvent such as dimethylformamide or dimethylsulfoxide. The opening of the epoxide 13 with SUBSTITUTE SHEET (RULE 26) compound 4 to give compound 6 is optimally performed over a period of 2-7 hours at. 50 - 60 °C.
In Step 5 t:he car_bobenzyloxy group can be removed to give the free amine 7.. This can be done using HBr in acetic acid using cosol.vents such as halocarbons. It can also be performed using halide's of boron such as BBrj and BC13 or alkyl substituted boron halides such as dimethylboron bromide in halocarbon solvents like chloroform and dichloromethane at temperatures ranging from 0 °C up to ambient temperature. Alternatively, the carbobenzyloxy group can be removed by hydrolysis using aqueous/alcoholic solutions of metal hydroxides like barium, sodium, lithium or potassium hydroxide at temperatures above ambient for periods of hours.
Step 6a is the coupling of benzoic acid derivatives of formula 8 to give 9a. In Formula 8, Q can be a leaving group. Q can be any of: the leaving groups discussed above for Group J. The compounds of formula 8 where Q = OH or Cl are commercially available from EMS Dottikon, Lenzburg, Switzerland and Sugai Chemical Industries, Ltd. in Japan.
The coupling can be carried out in a variety of ways, depending on the identity of Q. When a free acid is used (Q
- OH), the coupling ca.n be performed using carbodiimide based methods utilizing any of the common reagents of this class including dicyclohexylcarbodiimide or related dialkylcarbodiimides, EDC (salts of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide) or related water soluble reagents along with an organic amine base in polar organic solvents such as dioxane, DMF, NMP and acetonitrile in the presence of an N-hydroxyheterocyclic including N-hydroxysuccinimide or 3-hydroxybenzotriazole. When Q = a halogen or pseudohalogen, the coupling may be performed in most common organic solvents such as THF, diethyl ether, dioxane, methyl t-butyl ether or other ethers; acetone, cyclohexanone, methyl isobutylketone and other ketones;
esters such as ethyl, methyl and isopropyl acetate;
SUBSTITUTE SHEET (RULE 26) halogenated solvents such as halogenated urethanes and ethanes, chlorobenzene and other halogenated benzenes;
nitrites such acetonitrile and propionitrile; lower alcohols such as ethanol, isopropanol, t-butanol and related alcohols, and polar organic solvents such as dimethylformamide, dimethylsulfoxide, N-methyl-2-pyrrollidone and related amide-containing solvents. A base is frequently used and may be any of a number of inorganic bases such as metal hydroxides, bicarbonates and carbonates or organic bases such as amines like triethylamine, diethylamine, diethyl isopropylamine, DABCO or related di-or trialkylamines, as well as amidine bases like DBU and DBN.
Acetate removal is accomplished in step 6b with aqueous or alcoholic solutions of inorganic bases such as metal hydroxides, carbonates and bicarbonates at ambient temperatures up to 100 °C. If there is a protected functionality on the carboxamide group bonded to the perhydroisoquinoline ring system, it is best removed at this point (during or after step 6b). The, nature of this step is dependent on the exact identity of the protecting group.
A preferred method for accomplishing the entire process shown in Scheme I is shown in Scheme II.
The Cbz-protected amino acid 15 was coupled with the amine 22 to give the amide 16. The Cbz group was removed by hydrogenation to SUBSTITUTE SHEET (RULE 26) Scheme 11. Synthesis of Amidc 21 H ~ H
I
H COM-I-t-Bu COOIH ~l7 fMS
OII
N 1. 6 N aq. HC1 ~ N H=N ~ ~~ H2 H Me H -~. H ~ N 5% Pd~C 1 N H
H
2. CI~I H FDC, f-Ipgt~H20 H EtOH
H
Pattptltnisoquinoune STEP A STEP 8 -STEP C "
sPh Me C» CI SPh p~ 1V H ~ I \ COC1 OH ~ _ ()I1 SPh N
Me 50°/ aq. thpt-1 ~ pl I ~ 20 CLlotvalaohd Cbal W N H
OH HzN N
IJaCXI, IPA H IPA ~ ~i fi Et3N, THF, EtOH;
Ij ~ then 50%aq. N~OII
STEP D '8 STEP E '9 STEP F
H
SPh Me Oti H OH N . H
H
give the amine :L7. This was coupled with the chloroalcohol via the epoxide using the in situ procedure to give the adduct 18. Com~entional deprotection with base and coupling of the free primary amine with the acid chloride 20 gave rise to amide 2:1. Details of this process are provided below in ExamplE~s 1 A to F. The lettering A to F in Scheme II corresponds i.o Examples 1 A to F below.
The following Examples illustrate aspects of the invention. There examples are for illustrative purposes and are not intended to limit the scope of the invention.
Abbreviations for the terms melting point, nuclear magnetic resonance spectra, electron impact mass spectra, field desorption mass spectra, fast atom bombardment mass spectra, infrared spectra, ultraviolet spectra, elemental analysis, high performance liquid chromatography, and thin layer chromatography are, respectively, m.p., NMR, EIMS, MS(FD), MS(FAB), IR, W, Analysis, HPLC, and TLC. In addition, the absorption maxima listed for the IR spectra are those of ini=erest, not all maxima observed.
SUBSTITUTE SHEET (RULE 26) In conjunction with the NMR spectra, the following abbreviations are used: singlet (s), doublet (d), doublet of doublets (dd) , triplet (t) , quartet (q) , multiplet (m) , doublet of multiplets (dm), broad singlet (br.s), broad doublet (br.d), broad triplet (br.t), and broad multiplet (br.m). J indicates the coupling constant in Hertz (Hz).
Unless otherwise noted, NMR data refer to the free base of the subject compound.
NMR spectra were obtained on a General Electric QE-300 300MHz instrument. Chemical shifts are expressed in b values in ppm. Mass spectra were obtained on a VG ZAB-3 Spectrometer at the Scripps Research Institute, La Jolla, CA. Infra-red spectra were recorded on a Midac Corporation spectrometer. UV spectra were obtained on a Varian,Cary 3E
instrument. Thin layer chromatography was carried out using silica plates available from E. Merck. Melting points were measured on a Mettler FP62 instrument and are uncorrected.
Example 1 Procedures for the Synthesis of Amide of Formula 21 [3S- [2 (2S*, 3S*) , 3 alpha, 4a beta, 8a beta] ] -N- (l, 1-dimethyl-2-hydroxyethyl)decahydro-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-(phenylthio)butyl]-3-isoquinolinecarboxamide H
SPh O N
Me O ~ ~OH
HO ~ Me Me N
H OH
i A. Perhydroisoquinoline (26.4 g, 111 mmol} (commerically available from NSC Technologies (Chicago, IL) or Procos SpA
(Milan, Italy)) was suspended in water (200 mL) and concentrated aqueous HC1 (200 mL). This mixture was heated SUBSTITUTE SHEET (RULE 26) to reflux and stirred for 3 days, during which time it went into solution. The solvents were removed under reduced pressure to give a light yellow solid. The solid was slurried in 2-propanol (200 mL) and filtered. The filtrate was evaporated under reduced pressure to an oil. EtOAc (100 mL) and water (100 mL) were added and the pH of the solution was brought to 8.0 by the addition of 2 N aqueous KOH.
Benzyl chloroformate (15.8 mL, 111 mmol) was added dropwise over 30 minutes and the pH was kept between 7 and 8 by the addition of 2 N aqueous KOH. The mixture was stirred at room temperature for 18 hours. EtOAc (200 mL) was added and the organic layer was washed with 1 N aqueous HC1 (100 mL), and brine (100 mL). The organic layer was dried (MgS09), filtered, and evaporated under reduced pressure to an oil.
The product was purified by silica gel chromatography, eluting with 1:1 40-60 petroleum ether/EtOAc followed by 1000 EtOAc. The fractions containing product were collected and evaporated under reduced pressure to give the compound 15 (11.3 g, 32%) as a colorless oil: 1H NMR (300 MHz, CDC13) ~ 7.43-7.28 (m, 5 H), 5.17 (br s, 2 H), 4.76 (m, 1 H), 3.79 (m, 1 H), 3.33 (m, 1 H), 2.19 (m, 1 H), 1.96 (m, 1 H), 1.88-1.15 (m, 10 H) .
B. 1-Hydroxyb~~nzotriazole (4.2 g, 31.4 mmol) and EDC (6.0 g, 31.4 mmol) ware added to a solution of acid 15 (8.3 g, 26.2 mmol) in DI~IF (128 mL) at ambient temperature. The mixture was hea":,ed at 80° C for 10 minutes. 1,1-Dimethyl-2-trimethylsilylo:Kyethylamine (5.1 g, 31.4 mmol, prepared from 1,1-dimethyl-2-lzydroxyethylamine (Aldrich Chemical Co.) and hexamethyldisil;~zane (Aldrich Chemical Co.)) by heating the mixture neat under reflux for several hours followed by evaporation of the volatile components was added and the solution was he~~ted at 80° C for 17 hours. The yellow solution was po~ired into EtOAc (250 mL) and 2 N aqueous HCl (250 mL). Afte:r stirring for 10 minutes EtOAc (750 mL) was added and the mixture was washed with H20 (3 x 500 mL) and brine (1 x 250 mL). The combined aqueous layers were extracted with 7~tOAc (1 x 250 mL). The combined organic layers were dried (NazS04) and purified by flash SUBSTITUTE SHEET (RULE 26) chromatography (50/50 EtOAc/hexanes) to give the compound 16 as a colorless oil (7.9 g, 78%): 1H NMR (300 MHz, CD30D) S
7.36 (m, 5 H), 5.20 (d, J = 8.1 Hz, 1 H), 5.10 (m, 1 H), 4.53 (m, 1 H), 3.78 (dd, J = 13.2, 4.4 Hz, 1 H), 3.60 (m, 2 H), 3.48 (d, J = 10.7 Hz, 1 H), 2.15-1.25 (m, 12 H), 1.31 (s, 3 H) , 1.29 (s, 3 H) .
C. A mixture of carbamate 16 (7.9 g, 20.4 mmol) and 5%
palladium on carbon (Pd/C)(1.6 g) was hydrogenated at 50 psi H~ in absolute EtOH (110 mL) at ambient temperature for 18 hours. The mixture was filtered through Celite and evaporated in vacuo to give amine 17 as a white, crystalline solid: 'H NMR (300 MHz, CD30D) b 3.63 (q, J = 7.0 Hz, 2 H), 3.34 (m, 1 H), 3.27 (dd, J = 11.8, 3.3 Hz, 1 H), 2.91 (m, 1 H), 2.02-1.15 (m, 12 H), 1.32 (s, 3 H), 1.31 (s, 3 H).
D. Aqueous 10.2 N NaOH (2.4 mL, 24.5 mmol) was added to a warm (27 °C) suspension of chloroalcohol (obtained from Kaneka Industries in Japan)(10.4 g, 28.6 mmol) in isopropanol (IPA)(104 mL) with mechanical stirring. After 1 hour 1 N aqueous HC1 in IPA (prepared by addition of 1 mL of concentrated aqueous HCl to 12 mL of IPA) approximately (ca.) 1 mL) was added to neutralize (pH = 7). Amine 17 (5.2 g, 20.4 mmol) was added as a solution in IPA (50 mL) and the thin suspension was heated at 60° C for 10 hours. The IPA
was removed in vacuo. The residue was diluted with EtOAc (150 mL) and washed with Hz0 (2 x 50 mL) , saturated aqueous NaHC03 (1 x 50 mL), and brine (1 x 50 mL). The combined aqueous layers were extracted with EtOAc (1 x 25 mL). The combined organic layers were dried (NazSO~) and purified by flash chromatography (75/25 EtOAc/hexanes, then EtOAc) to give the compound 18 as a white solid (8.98 g, 76%): 1H NMR
(300 MHz, CD30D) d 7.33 (m, 10 H) , 5.08 (AB, JAB = 12.2 Hz, ~uAB = 12.1 Hz, 2 H), 3.96, (m, 2 H), 3.56 (q, J = 7.3 Hz, 2 H), 3.50, (m, 1 H), 3.20 (dd, J = 13.6, 9.2 Hz, 1 H), 3.03 (m, 1 H) , 2.64 (m, 2 H) , 2.20-1.20 (m, 14 H) , 1.28 (s, 6 H) .
SUBSTITUTE SHEET (RULE 26) E. 50% aqueous NaOH (2.7 g, 1.8 mL, 33.6 mmol) was added to a suspension of carbamate 18 (6.75 g, 11.6 mmol) in IPA
(34 mL) at ambient temperature. The mixture was heated under reflux for 12 hours. After cooling to ambient temperature, the mixture was diluted with methyl t-butyl ether (MTBE) (600 mL) and washed with H20 (2 x 250 mL) and brine (1 x 125 mL). T'he combined aqueous layers were extracted with MTBE (1 x 150 mL). The combined organic layers were dried (Naz;509) and evaporated in vacuo to give a mixture of compound 19 and benzyl alcohol as an oily white solid: -H NMR 0300 MH:z, CD30D) b 7.34 (m, 10 H) , 4.63 (s, 2 H), 3.81 (m, 1 H), 3.58 (m, 3 H), 3.03-2.60 (m, 5 H), 2.17 (m, 1 H) , 2.05 ('m, 1 H) , 1.87-1.05 (m, 12 H) , 1.30 (s, 3 H) , 1.28 (s, 3 H) .
F. Triethylami:ne (3.2 g, 4.3 mL, 31.2 mmol) was added to a solution of the mixture of amine 19 (4.7 g, 10.4 mmol theory from 18) and benzyl alcohol in EtOH (23 mL) at ambient temperature. A solution of 3-acetoxy-2-methylbenzoyl chloride (20)(obtained according to procedures set forth in U.S. Patent Application Serial No. 08/708,411, filed September 5, 1995, which is specifically incorporated by reference herein) (2.4 g, 11.5 mmol) in THF (4 mL) was added. After 2 :hours 50% aqueous NaOH (4.1 g, 2.8 mL, 52.2 mmol) was added ~~nd the mixture was heated under reflux for 1 hour. After c~~oling to ambient temperature, the mixture was neutralized to pH = 7 with 2 N aqueous HC1 (26 mL).
This mixture was diluted with EtOAc (500 mL) and washed with H20 (1 x 250 mL) , satuo~ated aqueous NaHC03 (2 x 250 mL) , Hz0 (1 x 250 mL), and brine (1 x 125 mL). The organic layer was dried (Na~S09) and purified by flash chromatography {75/25 EtOAc/hexanes) to give amide 21 as a white foam {1173-57A, 1 . 3 9 g, 23 % ) . T:ze 1H t~TMR indicated the presence of 11 wt EtOAc which coul~3 not be removed in vacuo.
SUBSTITUTE SHEET (RULE 26) Analysis:
1H NMR (300 MHz, CD~OD) S 7.53 (d, J = 7.3 Hz, 2 H} , 7.32 (t, J = 7.0 Hz, 2 H), 7.20 (t, J = 7.3 Hz, 1 H}, 7.06 (t, J =
8.1 Hz, 1 H}, 6.92 (d, J = 8.1 Hz, 1 H), 6.83 (d, J = 8.1 Hz, 1 H), 4.42 (m, 1 H), 4.08 (m, 1 H}, 3.61 (dd, J = 13.6, 4. 0 Hz, 1 H) , 3 .45 (AB, JAB = 11 .0 Hz, ~uAg = 18.0 Hz, 2 H) , 3.29 (dd, J = 13.6, 10.3 Hz, 1 H), 3.10 (m, 1 H), 2.66 (m, 2 H), 2.28 (s, 3 H), 2.22 (m, 2 H), 2.04 (m, 1 H), 1.86-1.20 (m, 11 H) , 1.19 (s, 3 H) , 1 .18 (s, 3 H) .
1'C NMR (75.5 MHz, CD30D) ~ 175.7, 172.5, 155.9, 138.8, 136.7, 129.8, 128.9, 126.3, 126.0, 122.4, 118.4, 115.9, 70.3, 69.9, 68.2, 59.3, 58.8, 54.9, 53.0, 36.5, 34.2, 34.1, 31.1, 30.7, 26.4, 26.0, 23.1, 23.0, 20.8, 12.1.
Example 2 HIV Protease inhibition activity and anti HIV activity in cell culture of compound 21 Tight binding kinetics analysis was used to determine the magnitude of the Ki values of compound 21. The Ki= 5.6 ~
0.91nM.
Methods Expression of HIV-1 protease HIV-1 protease gene was isolated from the viral strain IIIB (Ratner, L. et al., Nature, 316, 227-284 (1985)). In order to increase the stability of purified protease (Rose, J.R, et al., J. Biol. Chem., 268, 11939-11945 (1993)), the glutamine residue at position 7 (Q7) was mutated to serine (S) by replacing the 33 base pairs segment between the NdeI
and BstEII sites of the protease gene sequence with synthetic oligonucleotides encoding the Q75 mutation. The modified gene sequence was inserted into the plasmid vector pGZ (Menge, K.L. et la., Biochemistry, 34:15934-15942 (1995) under the control of phage T7 promoter. The resulting SUBSTITUTE SHEET (RULE 26) construct, pGZ/HP-19Q'7S#9, was transformed into E. coli strain BL21(DE3) purchased from Novagen, Inc.
Expression of HIV-1 PR: Cultures were grown in 2YT
media (1.6% Try>ticase Pepton, 1% Yeast extract, 0.5 % NaCl at an initial pH 7.5) containing 200 ~g/L ampicillin in 100 L fermentor (Biolafitt:e SA) at 37°C for 5 hours and then induced by addition of: 1 mM IPTG {Isopropyl-(3-D-thiogalactopyran.oside). The temperature of the culture during induction. was raised to 42°C to increase accumulations of the recombinant HIV-1 protease as insoluble inclusion bodies. After 2 hours at 42°C, cells were harvested by crcssflow filtration using Pellicon 0.1 ~,m VVPPOOOC5 cassette #10 {Millipore) and the cell paste was stored frozen at -70°C'.
Purification of Recombinant HIV-1 Protease: All steps unless otherwise indicated were carried out at 4°C. Protein concentrations were dE:termined using BioRad protein assay solution with bovine ~;erum albumin (BioRad, Richmond, CA) as a standard. Chromatographic steps and the purity of HIV PR
was analyzed by sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE). Final purity of HIV-PR was > 98o. Typical final yield from each 100 L culture was 120 mg.
Cell paste from 1.00L culture was resuspended in 300 mL
of lysis buffer (50 mM Tris-C1 pH 8.0, 25 mM NaCl, 20 mM 2-mercaptoethanol) and microfluidized in Microfluidics Corporation fluidizer at 22,000 psi. The crude cell lysate was clarified by centrifugation at 14,000 rpm for 20 minutes. HIV PR was found predominantly in the pellet in the form of inclusion bodies. The inclusion bodies were subsequently washed multiple times in the lysis buffer containing in addition 0.1% Trition-X100 and 1 M urea, and after each washing procedure, the inclusion bodies were SUBSTITUTE SHEET (RULE 26) pelleted by centrifugation at 5,000 rpm for 20 minutes.
Purified inclusion bodies were solubilized in buffer containing 50 mM Tris-C1, pH 8.0, 25 mM NaCl, 20 mM 2-mercaptoethanol, and 8 M urea. Solution was clarified by centrifugation at 14,000 rpm and applied at room temperature to a 300 mL Fast Flow Q-Sepharose column (Pharmacia, Piscataway, NJ) equilibrated with the same buffer. Under these conditions HIV PR did not bind to the column and essentially pure enzyme was found in the flow-through fractions. To renature the protein, the fractions from Fast Flow Q-Sepharose column were dialyzed against three changes of buffer containing 25 mM NaH2P04 pH 7.0, 25 mM NaCl, 10 mM
DTT and 10o glycerol. After refolding, small quantities of precipitated material were removed by centrifugation and resultant enzyme preparation were concentrated, dialyzed against 0.5 M NaCl, 50 mM MES pH 5.6, 10 mM DTT, frozen in small aliquots at "'2 mg/mL and stored at -70°.
Tight-Binding Kinetics Assay and Analysis Proteolytic activity of purified HIV-1 protease was measured using a modified chromogenic assay developed by Richards at al. (Richards, A.D. et al. J. Biol. Chem., 256, 773-7736 (1990)). The synthetic peptide His-Lys-Ala-Arg-Val-Leu-Phe(paraN02)-Glu-Ala-Nle-Ser-NHz (American Peptide Company) (Nle is norleucine) was used as a substrate. The assay was carried out in 0.5 M NaCl, 50 mM MES pH 5.6, 5 mM
DDT, and 2o DMSO at 37°C. Cleavage of the scissile bond between leucine and paranitro-phenylalanine (Phe para-N02) was assayed by spectrophotometric monitoring of the decrease on absorbance at 305 nm. Initial velocity was determined as the rate of decline of absorbance during the first 100 seconds of the enzymatic reaction. Under these conditions, and using Q7S HIV-1 protease, the Michaelis constant (Km) for this substrate is 59 ~ 17 /.cM.
SUBSTITUTE SHEET (RULE 26j For determ:inatio:n of the inhibition of compound 21, a saturating concE:ntration of substrate of 200 uM was used.
Between 13 and 20 con~~entrations of inhibitors were evaluated and the velocity of reaction was measured at each concentration a:~ desc:ribed above. The apparent Ki (Ki app), set forth above,. was determined by computer assisted non-linear least square fitting of the data to the tight binding equation of Mor~:ison (Morrison, J.F., Biochem. Biophys.
Acta, 185, 269-~?86 (1963) ) .
Example 3 Antiviral activity of compound 21 against HIV-1 in cell culture Cells and virus strains:
The CEM-SS and MT-2 human T cell lines and HIV-1 strains RF and 7:IIB we=re obtained from the AIDS Research and Reference Progr~im, Division of AIDS, NIAID, and NIH.
Cell protection assavs_ The inhibitory ei=fects of each agent on HIV-1 replication were measured by the MTT dye reduction method (Alley, M.C. et al., Cancer Res. 48: 589-601 (1988)).
Compounds were dissolved in DMSO at a concentration of 40 mg/ml then diluted 1:200 in culture medium (RPMI, supplemented with 10% fetal bovine serum). From each diluted stock, 1.00 ~1 was added to a 96-well plate and serial half-log dilutions were prepared. In separate tubes, MT-2 cells and C'EM-SS cells were infected with HIV-1 IIIB or HIV-1 RF at a multiplicity of infection (m.o.i.) of 0.01 and 0.03, respectively. Following a 4-hour adsorption period, 100 ~.1 of infected or uninfected cells were added to the .
wells of the drug containing plate to give a final concentration of 1 x L09 cells/well. Six days (CEM-SS
cells) or 7 days; (MT-2 cells) later, MTT (5 mg/ml) was added to test plates and the amount of formazan produced was SUBSTITUTE SHEET (RULE 26) quantified spectrophotometrically at 570 nm. Data were expressed as the percentage of formazan produced in drug-treated cells compared to formazan produced in wells of uninfected, drug-free cells. The EDSO was calculated as the concentration of drug that increased the percentage of formazan production in infected, drug-treated cells to 500 of that produced by uninfected, drug-free cells.
Cytotoxicity (TCSp) was calculated as the concentration of drug that decreased the percentage of formazan produced in uninfected, drug-treated cells to 50% of that produced in uninfected, drug-free cells. The therapeutic index (TI) was calculated by dividing the cytotoxicity (TCSO) by the antiviral efficacy (ED50).
Table 1 Antiviral Activity and Cytotoxicity Evaluations of Compound in an Acute Infection of CEM-SS cells with HIV-1 RF
Compound ED50 ED95 TC50 Therapeutic (nM) (nM) (~M) index a 21 34.2 154.1 96.6 2825 azidophymidine 52.3 543.1 >374.5 >7161 (AZT) dideoxycytidine 94.70 142.0 37.69 398 (ddC) Therapeutic index = Cytotoxicity (TCS~) . Antiviral activity (EDSO) -SUBSTITUTE SHEET (RULE 26) Table 2 Antiviral Activity and Cytotoxicity Evaluations of Compound in an Acute Infection of MT-2 cells with HIV-1 IIIB
Compound ED~~~ ED93 TC50 Therapeu (nM) (nM) (~,M) tic 21 85.6 ND 92.6 1082 AZT 430.7 ND 109.4 254 ddC 5924 ND 176.3 30 aTherapeutic index = C'ytotoxicity (TCSp) . Antiviral activity (ED50) .
As noted ar~ove, t:he compounds of the present invention are useful for inhibit:ing HIV protease, which is an enzyme associated with viral component production and assembly. An embodiment of th.e pre~~ent invention is a method of treating HIV infection comprising administering to a host or patient, such as a primate, an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof.
Another embodiment of the present invention is a method of treating AIDS comprising administering to a host or patient an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof. A further embodiment of the pre~~ent invention is a method of inhibiting HIV proteae;e comprising administering to an HIV
infected cell or a ho~;t or patient, such as a primate, infected with HIV, an effective amount of a compound of formula (1) or a pharmaceutically acceptable salt thereof.
The term "effecti.ve amount" means an amount of a compound of formula (9) or its pharmaceutically acceptable SUBSTITUTE SHEET (RULE 26) salt that is effective to inhibit the HIV protease mediated viral component production and assembly. The specific dose of compound administered according to this invention to obtain therapeutic or inhibitory effects will, of course, be determined by the particular circumstances surrounding the case, including, for example, the compound administered, the route of administration, the condition being treated and the individual host or patient being treated. An exemplary daily dose (administered in single or divided doses) contains a dosage level of from about 0.01 mg/kg to about 50 mg/kg of body weight of a compound of this invention.
Preferred daily doses generally are from about 0.05 mg/kg to about 40 mg/kg and, more preferably, from about 1.0 mg/kg to about 30 mg/kg.
The compounds of the invention may be administered by a variety of routes, including oral, rectal, transdermal, subcutaneous, intravenous, intramuscular and intranasal routes. The compounds of the present invention are preferably formulated prior to administration. Therefore, another embodiment of the present invention is a pharmaceutical composition or formulation comprising an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, such as a diluent or excipient therefor.
The active ingredient preferably comprises from 0.1% to 99.9% by weight of the formulation. By "pharmaceutically acceptable" it is meant that the carrier, such as the diluent or excipient, is compatible with the other ingredients of the formulation and not deleterious to the host or patient.
Pharmaceutical formulations may be prepared from the compounds of the invention by known procedures using known-SUBSTITUTE SHEET (RULE 26) WO 9$140357 PCT/US9$/04735 and readily available ingredients. In making the compositions of the present invention, the active ingredient will usually be admixed with a carrier, or diluted by a carrier, or enclosed within a carrier, which may be in the form of a capsu=.e, sa~~het, paper or other suitable container. 49hen the carrier serves as a diluent, it may be a solid, semi-solid o:r liquid material which acts as a vehicle, excipient or medium for the active ingredient.
Thus, the compo:~itions can be in the form of tablets, pills, powders, lozenge's, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointmf_nts (containing, for example, up to loo by weight of: the <~ctive compound), soft and hard gelatin capsules, suppo~~itories, sterile injectable solutions, sterile packaged powders and the like.
The following formulation examples are illustrative only and are not; intended to limit the scope of the invention. The term "active ingredient" represents a compound of formula (9) or a pharmaceutically acceptable salt thereof.
SUBSTITUTE SHEET (RULE 26) Formulation 1 Hard gelatin capsules are prepared using the following ingredients:
Quantity (m~/capsule) Active ingredient 250 Starch, dried 200 Magnesium stearate 10 Total 460 mg Formulation 2 A tablet is prepared using the ingredients below:
Quantity (mc~/tablet) Active ingredient 250 Cellulose, microcrystalline 400 Silicon dioxide, fumed 10 Stearic acid 5 Total 665 mg The components are blended and compressed to form tablets each weighing 665 mg.
SUBSTITUTE SHEET RULE 26~
Formulation 3 An aerosol so:Lution is prepared containing the following components:
Weight Active ingredient 0.25 Methanol 25.75 Propellant 22 (Chlorodifluoromethane) 74.00 Tota 100.00 The active compound is mixed with ethanol and the mixture added to a portion of tl:~e propellant 22, cooled to -30°C and transferred to a i=filling device. The required amount is then fed to a stainles:~ steel container and diluted with the remainder of the propel:Lant. The valve units are then fitted to the container.
Formulation 4 Tablets, each containing 60 mg of active ingredient, are made as follows:
Quantity (mg/tablet) Active ingredient 60 Starch 45 Microcrystalline cellulose 35 Polyvinylpyrrolidone (as loo solution in waiver) 4 Sodium carboxymethyl sta=rch 4.5 Magnesium stearate 0.5 Talc 1 Total 150 SUBSTITUTE SHEET (RULE 26) The active ingredient, starch and cellulose are passed through a No. 45 mesh U.S. sieve and mixed thoroughly. The aqueous solution containing polyvinylpyrrolidone is mixed with the resultant powder, and the mixture then is passed through a No.
14 mesh U.S. sieve. The granules so produced are dried at 50°C
and passed through a No. 18 mesh U.S. sieve. The sodium carboxymethyl starch, magnesium stearate and talc, previously passed through a No. 60 mesh U.S. sieve, are then added to the granules which, after mixing, are compressed on a tablet machine to yield tablets each weighing 150 mg.
Formulation 5 Capsules, each containing 80 mg of active ingredient, are made as follows:
Quantity (mg/capsule) Active ingredient 80 mg Starch 59 mg Microcrystalline cellulose 59 mg Magnesium stearate 2 mg Total 200 mg The active ingredient, cellulose, starch and magnesium stearate are blended, passed through a No. 45 mesh U.S. sieve, and filled into hard gelatin capsules in 200 mg quantities.
Formulation 6 Suppositories, each containing 225 mg of active ingredient, are made as follows:
Active ingredient 225 mg Saturated fatty acid glycerides 2.000 mg Total 2,225 mg The active ingredient is passed through a No. 60 mesh U.S.
sieve and suspended in the saturated fatty acid glycerides previously melted using the minimum heat necessary. The SUBSTITUTE SHEET (RULE 26) WO 98!40357 PCT/US98/04735 mixture is then poured into a suppository mold of nominal 2 g capacity and allowed to cool.
Formulation 7 Suspensions, a>.ach containing 50 mg of active ingredient per 5 ml dose, are made as follows:
Active ingredient 50 mg Sodium carboxymethyl cellulose 50 mg Syrup 1.25 ml Benzoic acid solution 0.10 ml Flavor q,v, Color q.v, Purified water to total 5 ml The active ingredient is passed through a No. 45 mesh U.S.
sieve and mixed with the sodium carboxymethylcellulose and syrup to form a smooth paste. The benzoic acid solution, flavor and color are diluted with a portion of the water and added, with stirring. Sui=ficient water is then added to produce the requirE~d volume .
Formulation 8 An intravenou~o formulation is prepared as follows:
Active ingredient 100 mg Isotonic saline 1,00() mL
The solution of the: above ingredients generally is administered intravenously to a subject at a rate of 1 ml per minute.
SUBSTITUTE SHEET (RULE 26) Formulation 9 A tablet is prepared using the ingredients below:
Quantity (ma/tablet) Active ingredient 292 mg calcium silicate 146 mg crospovidone 146 mg Magnesium stearate 5 mg Total 589 mg SUBSTITUTE SHEET (RULE 26)
1'C NMR (75.5 MHz, CD30D) ~ 175.7, 172.5, 155.9, 138.8, 136.7, 129.8, 128.9, 126.3, 126.0, 122.4, 118.4, 115.9, 70.3, 69.9, 68.2, 59.3, 58.8, 54.9, 53.0, 36.5, 34.2, 34.1, 31.1, 30.7, 26.4, 26.0, 23.1, 23.0, 20.8, 12.1.
Example 2 HIV Protease inhibition activity and anti HIV activity in cell culture of compound 21 Tight binding kinetics analysis was used to determine the magnitude of the Ki values of compound 21. The Ki= 5.6 ~
0.91nM.
Methods Expression of HIV-1 protease HIV-1 protease gene was isolated from the viral strain IIIB (Ratner, L. et al., Nature, 316, 227-284 (1985)). In order to increase the stability of purified protease (Rose, J.R, et al., J. Biol. Chem., 268, 11939-11945 (1993)), the glutamine residue at position 7 (Q7) was mutated to serine (S) by replacing the 33 base pairs segment between the NdeI
and BstEII sites of the protease gene sequence with synthetic oligonucleotides encoding the Q75 mutation. The modified gene sequence was inserted into the plasmid vector pGZ (Menge, K.L. et la., Biochemistry, 34:15934-15942 (1995) under the control of phage T7 promoter. The resulting SUBSTITUTE SHEET (RULE 26) construct, pGZ/HP-19Q'7S#9, was transformed into E. coli strain BL21(DE3) purchased from Novagen, Inc.
Expression of HIV-1 PR: Cultures were grown in 2YT
media (1.6% Try>ticase Pepton, 1% Yeast extract, 0.5 % NaCl at an initial pH 7.5) containing 200 ~g/L ampicillin in 100 L fermentor (Biolafitt:e SA) at 37°C for 5 hours and then induced by addition of: 1 mM IPTG {Isopropyl-(3-D-thiogalactopyran.oside). The temperature of the culture during induction. was raised to 42°C to increase accumulations of the recombinant HIV-1 protease as insoluble inclusion bodies. After 2 hours at 42°C, cells were harvested by crcssflow filtration using Pellicon 0.1 ~,m VVPPOOOC5 cassette #10 {Millipore) and the cell paste was stored frozen at -70°C'.
Purification of Recombinant HIV-1 Protease: All steps unless otherwise indicated were carried out at 4°C. Protein concentrations were dE:termined using BioRad protein assay solution with bovine ~;erum albumin (BioRad, Richmond, CA) as a standard. Chromatographic steps and the purity of HIV PR
was analyzed by sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE). Final purity of HIV-PR was > 98o. Typical final yield from each 100 L culture was 120 mg.
Cell paste from 1.00L culture was resuspended in 300 mL
of lysis buffer (50 mM Tris-C1 pH 8.0, 25 mM NaCl, 20 mM 2-mercaptoethanol) and microfluidized in Microfluidics Corporation fluidizer at 22,000 psi. The crude cell lysate was clarified by centrifugation at 14,000 rpm for 20 minutes. HIV PR was found predominantly in the pellet in the form of inclusion bodies. The inclusion bodies were subsequently washed multiple times in the lysis buffer containing in addition 0.1% Trition-X100 and 1 M urea, and after each washing procedure, the inclusion bodies were SUBSTITUTE SHEET (RULE 26) pelleted by centrifugation at 5,000 rpm for 20 minutes.
Purified inclusion bodies were solubilized in buffer containing 50 mM Tris-C1, pH 8.0, 25 mM NaCl, 20 mM 2-mercaptoethanol, and 8 M urea. Solution was clarified by centrifugation at 14,000 rpm and applied at room temperature to a 300 mL Fast Flow Q-Sepharose column (Pharmacia, Piscataway, NJ) equilibrated with the same buffer. Under these conditions HIV PR did not bind to the column and essentially pure enzyme was found in the flow-through fractions. To renature the protein, the fractions from Fast Flow Q-Sepharose column were dialyzed against three changes of buffer containing 25 mM NaH2P04 pH 7.0, 25 mM NaCl, 10 mM
DTT and 10o glycerol. After refolding, small quantities of precipitated material were removed by centrifugation and resultant enzyme preparation were concentrated, dialyzed against 0.5 M NaCl, 50 mM MES pH 5.6, 10 mM DTT, frozen in small aliquots at "'2 mg/mL and stored at -70°.
Tight-Binding Kinetics Assay and Analysis Proteolytic activity of purified HIV-1 protease was measured using a modified chromogenic assay developed by Richards at al. (Richards, A.D. et al. J. Biol. Chem., 256, 773-7736 (1990)). The synthetic peptide His-Lys-Ala-Arg-Val-Leu-Phe(paraN02)-Glu-Ala-Nle-Ser-NHz (American Peptide Company) (Nle is norleucine) was used as a substrate. The assay was carried out in 0.5 M NaCl, 50 mM MES pH 5.6, 5 mM
DDT, and 2o DMSO at 37°C. Cleavage of the scissile bond between leucine and paranitro-phenylalanine (Phe para-N02) was assayed by spectrophotometric monitoring of the decrease on absorbance at 305 nm. Initial velocity was determined as the rate of decline of absorbance during the first 100 seconds of the enzymatic reaction. Under these conditions, and using Q7S HIV-1 protease, the Michaelis constant (Km) for this substrate is 59 ~ 17 /.cM.
SUBSTITUTE SHEET (RULE 26j For determ:inatio:n of the inhibition of compound 21, a saturating concE:ntration of substrate of 200 uM was used.
Between 13 and 20 con~~entrations of inhibitors were evaluated and the velocity of reaction was measured at each concentration a:~ desc:ribed above. The apparent Ki (Ki app), set forth above,. was determined by computer assisted non-linear least square fitting of the data to the tight binding equation of Mor~:ison (Morrison, J.F., Biochem. Biophys.
Acta, 185, 269-~?86 (1963) ) .
Example 3 Antiviral activity of compound 21 against HIV-1 in cell culture Cells and virus strains:
The CEM-SS and MT-2 human T cell lines and HIV-1 strains RF and 7:IIB we=re obtained from the AIDS Research and Reference Progr~im, Division of AIDS, NIAID, and NIH.
Cell protection assavs_ The inhibitory ei=fects of each agent on HIV-1 replication were measured by the MTT dye reduction method (Alley, M.C. et al., Cancer Res. 48: 589-601 (1988)).
Compounds were dissolved in DMSO at a concentration of 40 mg/ml then diluted 1:200 in culture medium (RPMI, supplemented with 10% fetal bovine serum). From each diluted stock, 1.00 ~1 was added to a 96-well plate and serial half-log dilutions were prepared. In separate tubes, MT-2 cells and C'EM-SS cells were infected with HIV-1 IIIB or HIV-1 RF at a multiplicity of infection (m.o.i.) of 0.01 and 0.03, respectively. Following a 4-hour adsorption period, 100 ~.1 of infected or uninfected cells were added to the .
wells of the drug containing plate to give a final concentration of 1 x L09 cells/well. Six days (CEM-SS
cells) or 7 days; (MT-2 cells) later, MTT (5 mg/ml) was added to test plates and the amount of formazan produced was SUBSTITUTE SHEET (RULE 26) quantified spectrophotometrically at 570 nm. Data were expressed as the percentage of formazan produced in drug-treated cells compared to formazan produced in wells of uninfected, drug-free cells. The EDSO was calculated as the concentration of drug that increased the percentage of formazan production in infected, drug-treated cells to 500 of that produced by uninfected, drug-free cells.
Cytotoxicity (TCSp) was calculated as the concentration of drug that decreased the percentage of formazan produced in uninfected, drug-treated cells to 50% of that produced in uninfected, drug-free cells. The therapeutic index (TI) was calculated by dividing the cytotoxicity (TCSO) by the antiviral efficacy (ED50).
Table 1 Antiviral Activity and Cytotoxicity Evaluations of Compound in an Acute Infection of CEM-SS cells with HIV-1 RF
Compound ED50 ED95 TC50 Therapeutic (nM) (nM) (~M) index a 21 34.2 154.1 96.6 2825 azidophymidine 52.3 543.1 >374.5 >7161 (AZT) dideoxycytidine 94.70 142.0 37.69 398 (ddC) Therapeutic index = Cytotoxicity (TCS~) . Antiviral activity (EDSO) -SUBSTITUTE SHEET (RULE 26) Table 2 Antiviral Activity and Cytotoxicity Evaluations of Compound in an Acute Infection of MT-2 cells with HIV-1 IIIB
Compound ED~~~ ED93 TC50 Therapeu (nM) (nM) (~,M) tic 21 85.6 ND 92.6 1082 AZT 430.7 ND 109.4 254 ddC 5924 ND 176.3 30 aTherapeutic index = C'ytotoxicity (TCSp) . Antiviral activity (ED50) .
As noted ar~ove, t:he compounds of the present invention are useful for inhibit:ing HIV protease, which is an enzyme associated with viral component production and assembly. An embodiment of th.e pre~~ent invention is a method of treating HIV infection comprising administering to a host or patient, such as a primate, an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof.
Another embodiment of the present invention is a method of treating AIDS comprising administering to a host or patient an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof. A further embodiment of the pre~~ent invention is a method of inhibiting HIV proteae;e comprising administering to an HIV
infected cell or a ho~;t or patient, such as a primate, infected with HIV, an effective amount of a compound of formula (1) or a pharmaceutically acceptable salt thereof.
The term "effecti.ve amount" means an amount of a compound of formula (9) or its pharmaceutically acceptable SUBSTITUTE SHEET (RULE 26) salt that is effective to inhibit the HIV protease mediated viral component production and assembly. The specific dose of compound administered according to this invention to obtain therapeutic or inhibitory effects will, of course, be determined by the particular circumstances surrounding the case, including, for example, the compound administered, the route of administration, the condition being treated and the individual host or patient being treated. An exemplary daily dose (administered in single or divided doses) contains a dosage level of from about 0.01 mg/kg to about 50 mg/kg of body weight of a compound of this invention.
Preferred daily doses generally are from about 0.05 mg/kg to about 40 mg/kg and, more preferably, from about 1.0 mg/kg to about 30 mg/kg.
The compounds of the invention may be administered by a variety of routes, including oral, rectal, transdermal, subcutaneous, intravenous, intramuscular and intranasal routes. The compounds of the present invention are preferably formulated prior to administration. Therefore, another embodiment of the present invention is a pharmaceutical composition or formulation comprising an effective amount of a compound of formula (9) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, such as a diluent or excipient therefor.
The active ingredient preferably comprises from 0.1% to 99.9% by weight of the formulation. By "pharmaceutically acceptable" it is meant that the carrier, such as the diluent or excipient, is compatible with the other ingredients of the formulation and not deleterious to the host or patient.
Pharmaceutical formulations may be prepared from the compounds of the invention by known procedures using known-SUBSTITUTE SHEET (RULE 26) WO 9$140357 PCT/US9$/04735 and readily available ingredients. In making the compositions of the present invention, the active ingredient will usually be admixed with a carrier, or diluted by a carrier, or enclosed within a carrier, which may be in the form of a capsu=.e, sa~~het, paper or other suitable container. 49hen the carrier serves as a diluent, it may be a solid, semi-solid o:r liquid material which acts as a vehicle, excipient or medium for the active ingredient.
Thus, the compo:~itions can be in the form of tablets, pills, powders, lozenge's, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointmf_nts (containing, for example, up to loo by weight of: the <~ctive compound), soft and hard gelatin capsules, suppo~~itories, sterile injectable solutions, sterile packaged powders and the like.
The following formulation examples are illustrative only and are not; intended to limit the scope of the invention. The term "active ingredient" represents a compound of formula (9) or a pharmaceutically acceptable salt thereof.
SUBSTITUTE SHEET (RULE 26) Formulation 1 Hard gelatin capsules are prepared using the following ingredients:
Quantity (m~/capsule) Active ingredient 250 Starch, dried 200 Magnesium stearate 10 Total 460 mg Formulation 2 A tablet is prepared using the ingredients below:
Quantity (mc~/tablet) Active ingredient 250 Cellulose, microcrystalline 400 Silicon dioxide, fumed 10 Stearic acid 5 Total 665 mg The components are blended and compressed to form tablets each weighing 665 mg.
SUBSTITUTE SHEET RULE 26~
Formulation 3 An aerosol so:Lution is prepared containing the following components:
Weight Active ingredient 0.25 Methanol 25.75 Propellant 22 (Chlorodifluoromethane) 74.00 Tota 100.00 The active compound is mixed with ethanol and the mixture added to a portion of tl:~e propellant 22, cooled to -30°C and transferred to a i=filling device. The required amount is then fed to a stainles:~ steel container and diluted with the remainder of the propel:Lant. The valve units are then fitted to the container.
Formulation 4 Tablets, each containing 60 mg of active ingredient, are made as follows:
Quantity (mg/tablet) Active ingredient 60 Starch 45 Microcrystalline cellulose 35 Polyvinylpyrrolidone (as loo solution in waiver) 4 Sodium carboxymethyl sta=rch 4.5 Magnesium stearate 0.5 Talc 1 Total 150 SUBSTITUTE SHEET (RULE 26) The active ingredient, starch and cellulose are passed through a No. 45 mesh U.S. sieve and mixed thoroughly. The aqueous solution containing polyvinylpyrrolidone is mixed with the resultant powder, and the mixture then is passed through a No.
14 mesh U.S. sieve. The granules so produced are dried at 50°C
and passed through a No. 18 mesh U.S. sieve. The sodium carboxymethyl starch, magnesium stearate and talc, previously passed through a No. 60 mesh U.S. sieve, are then added to the granules which, after mixing, are compressed on a tablet machine to yield tablets each weighing 150 mg.
Formulation 5 Capsules, each containing 80 mg of active ingredient, are made as follows:
Quantity (mg/capsule) Active ingredient 80 mg Starch 59 mg Microcrystalline cellulose 59 mg Magnesium stearate 2 mg Total 200 mg The active ingredient, cellulose, starch and magnesium stearate are blended, passed through a No. 45 mesh U.S. sieve, and filled into hard gelatin capsules in 200 mg quantities.
Formulation 6 Suppositories, each containing 225 mg of active ingredient, are made as follows:
Active ingredient 225 mg Saturated fatty acid glycerides 2.000 mg Total 2,225 mg The active ingredient is passed through a No. 60 mesh U.S.
sieve and suspended in the saturated fatty acid glycerides previously melted using the minimum heat necessary. The SUBSTITUTE SHEET (RULE 26) WO 98!40357 PCT/US98/04735 mixture is then poured into a suppository mold of nominal 2 g capacity and allowed to cool.
Formulation 7 Suspensions, a>.ach containing 50 mg of active ingredient per 5 ml dose, are made as follows:
Active ingredient 50 mg Sodium carboxymethyl cellulose 50 mg Syrup 1.25 ml Benzoic acid solution 0.10 ml Flavor q,v, Color q.v, Purified water to total 5 ml The active ingredient is passed through a No. 45 mesh U.S.
sieve and mixed with the sodium carboxymethylcellulose and syrup to form a smooth paste. The benzoic acid solution, flavor and color are diluted with a portion of the water and added, with stirring. Sui=ficient water is then added to produce the requirE~d volume .
Formulation 8 An intravenou~o formulation is prepared as follows:
Active ingredient 100 mg Isotonic saline 1,00() mL
The solution of the: above ingredients generally is administered intravenously to a subject at a rate of 1 ml per minute.
SUBSTITUTE SHEET (RULE 26) Formulation 9 A tablet is prepared using the ingredients below:
Quantity (ma/tablet) Active ingredient 292 mg calcium silicate 146 mg crospovidone 146 mg Magnesium stearate 5 mg Total 589 mg SUBSTITUTE SHEET (RULE 26)
Claims (37)
1 . A compound of the formula (9):
wherein:
R and R' are independently selected from H, a substituted or unsubstituted alkyl-OR1 group, a cycloalkyl group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH
group, a heterocycle group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH group, an alkyl-NR2R3 group, or an alkyl-~ (X) (Y)R4 group, wherein R1 is H, a substituted or unsubstituted alkyl group, or an aryl group;
R2 and R3 are each independently selected from H, substituted or unsubstituted alkyl, cycloalkyl, heterocycle, and aryl groups, and acyl and sulfonyl groups;
R4 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group; and X and Y are each independently selected from =O and nothing;
or a pharmaceutically acceptable salt or solvate thereof.
wherein:
R and R' are independently selected from H, a substituted or unsubstituted alkyl-OR1 group, a cycloalkyl group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH
group, a heterocycle group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH group, an alkyl-NR2R3 group, or an alkyl-~ (X) (Y)R4 group, wherein R1 is H, a substituted or unsubstituted alkyl group, or an aryl group;
R2 and R3 are each independently selected from H, substituted or unsubstituted alkyl, cycloalkyl, heterocycle, and aryl groups, and acyl and sulfonyl groups;
R4 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group; and X and Y are each independently selected from =O and nothing;
or a pharmaceutically acceptable salt or solvate thereof.
2. A compound according to claim 1, wherein R is H, or a pharmaceutically acceptable salt or solvate thereof.
3. A compound according to claim 1, wherein when at least one of R and R' is an alkyl-OR1 group, R1 is H, or a pharmaceutically acceptable salt or solvate thereof.
4. A compound according to claim 1, wherein when at least one of R and R' is an alkyl-OR1 group, said alkyl-OR1 group is selected from -C(CH2)-CH2OH, -CH(CH2)CH2OH, -CH2CH2OH, -C(CH~)(CH2OH)2, -C(CH3)2-O-CH2-O-CH~, -C(CH3)~CH2-O-CH2-O-CH~, -C(CH2)2CH2-O-acyl, -C(CH3-4-S-CH2-O-CH3, -C(CH3)2CH2-~-CH2-O-CH3, -C(CH3)2-O-CH2-S-CH3, -C(CH~)2CH1-O-CH2-S-CH3, and -C(CH~)2CH3-S-acyl, or a pharmaceutically acceptable salt or solvate thereof.
5. A compound according to claim 1 wherein when at least one of R and R' is a cycloalkyl group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH group, said cycloalkyl group is selected from:
or a pharmaceutically acceptable salt or solvate thereof.
or a pharmaceutically acceptable salt or solvate thereof.
6.~A compound according to claim 1, wherein when at least one of R and R' is a heterocycle group substituted with a (C1-C6)alkyl group or a (C1-C6)alkyl-OH group, said heterocycle group is selected from:
wherein R1 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group, or an acyl or sulfonyl group, or a pharmaceutically acceptable salt or solvate thereof.
wherein R1 is H, a substituted or unsubstituted alkyl, cycloalkyl, heterocycle, or aryl group, or an acyl or sulfonyl group, or a pharmaceutically acceptable salt or solvate thereof.
7. A compound according to claim 1, wherein said compound has the formula 21:
or a pharmaceutically acceptable salt or solvate thereof.
or a pharmaceutically acceptable salt or solvate thereof.
8. A compound according to claim 2, wherein when R' is cycloalkyl group substituted with a (C1-C~)alkyl group or a (C1-C6)alkyl-OH group, said cycloalkyl group is selected from:
or a pharmaceutically acceptable salt or solvate thereof.
or a pharmaceutically acceptable salt or solvate thereof.
9. A salt according to claim 1, having the formula (9b):
10. A pharmaceutical composition comprising:
(a) an effective amount of compound of claim 1; and (b) a pharmaceutically acceptable carries thereof.
(a) an effective amount of compound of claim 1; and (b) a pharmaceutically acceptable carries thereof.
11. A pharmaceutical composition comprising:
(a) an effective amount of compound of claim 7; and (b) a pharmaceutically acceptable carrier therefor.
(a) an effective amount of compound of claim 7; and (b) a pharmaceutically acceptable carrier therefor.
12. A method of inhibiting HIV protease, comprising administering to a host an effective amount of compound of claim 1 or a pharmaceutically acceptable salt or solvate thereof.
13. A method of inhibiting HIV protease, comprising administering to a host an effective amount of compound of claim 7 or a pharmaceutically acceptable salt or solvate thereof.
14. A compound according to claim 1, which has a purity of more than 90%.
15. A compound according to claim 1, which has a purity of at least 95%.
16. A compound according to claim 1, which has a purity of at least 97%.
17. A compound according to claim 1, which has a purity of at least 99%.
18. A compound according to claim 7, which has a purity of more than 90%.
19. A compound according to claim 7, which has a purity of at least 95%.
20. A compound according to claim 7, which has a purity of at least 97%.
21. A compound according to claim 7, which has a purity of at least 99%.
22. A pharmaceutical composition according to claim 10, wherein the compound has a purity of more than 90%.
23. A pharmaceutical composition according to claim 10, wherein the compound has a purity of at least 95%.
24. A pharmaceutical composition according to claim 10, wherein the compound has a purity of at least 97%.
25. A pharmaceutical composition according to claim 10, wherein the compound has a purity of at least 99%.
26. A pharmaceutical composition according to claim 11, wherein the compound has a purity of more than 90%.
27. A pharmaceutical composition according to claim 11, wherein the compound has a purity of at least 95%.
28. A pharmaceutical composition according to claim 11, wherein the compound has a purity of at least 97%.
29. A pharmaceutical composition according to claim 11, wherein the compound has a purity of at least 99%.
30. A method according to claim 12, wherein the compound has a purity of move than 90%.
31. A method according to claim 12, wherein the compound has a purity of at least 95%.
32. A method according to claim 12, wherein the compound has a purity of at least 97%.
33. A method according to claim 12, wherein the compound has a purity of at least 99%.
34. A method according to claim 13, wherein the compound has a purity of more than 90%.
35. A method according to claim 13, wherein the compound has a purity of at least 95%.
36. A method according to claim 13, wherein the compound has a purity of at least 97%.
37. A method according to claim 13, wherein the compound has a purity of at least 99%.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81595197A | 1997-03-13 | 1997-03-13 | |
| US08/815,951 | 1997-03-13 | ||
| PCT/US1998/004735 WO1998040357A2 (en) | 1997-03-13 | 1998-03-12 | Hiv protease inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2284163A1 true CA2284163A1 (en) | 1998-09-17 |
Family
ID=25219265
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002284163A Abandoned CA2284163A1 (en) | 1997-03-13 | 1998-03-12 | Hiv protease inhibitors |
Country Status (35)
| Country | Link |
|---|---|
| EP (1) | EP0970055A2 (en) |
| JP (1) | JP2001516350A (en) |
| KR (1) | KR100511089B1 (en) |
| CN (1) | CN1179948C (en) |
| AP (1) | AP1358A (en) |
| AR (1) | AR012556A1 (en) |
| AU (1) | AU743078B2 (en) |
| BG (1) | BG63540B1 (en) |
| BR (1) | BR9808867A (en) |
| CA (1) | CA2284163A1 (en) |
| CO (1) | CO4940496A1 (en) |
| CZ (1) | CZ296647B6 (en) |
| EA (1) | EA002378B1 (en) |
| EE (1) | EE04114B1 (en) |
| GE (1) | GEP20022764B (en) |
| HR (1) | HRP980112A2 (en) |
| HU (1) | HUP0001380A3 (en) |
| IL (2) | IL131870A0 (en) |
| IS (1) | IS5176A (en) |
| MX (1) | MXPA99008395A (en) |
| MY (1) | MY117535A (en) |
| NO (1) | NO315555B1 (en) |
| NZ (1) | NZ337706A (en) |
| OA (1) | OA11196A (en) |
| PA (1) | PA8448801A1 (en) |
| PE (1) | PE58799A1 (en) |
| PL (1) | PL192786B1 (en) |
| SA (1) | SA98181116B1 (en) |
| SK (1) | SK283636B6 (en) |
| SV (1) | SV1998000038A (en) |
| TR (1) | TR199902508T2 (en) |
| TW (1) | TW200517112A (en) |
| UA (1) | UA57772C2 (en) |
| WO (1) | WO1998040357A2 (en) |
| ZA (1) | ZA982047B (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5484926A (en) * | 1993-10-07 | 1996-01-16 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
-
1998
- 1998-03-04 HR HR08/815,951A patent/HRP980112A2/en not_active Application Discontinuation
- 1998-03-11 ZA ZA982047A patent/ZA982047B/en unknown
- 1998-03-12 AR ARP980101104A patent/AR012556A1/en active IP Right Grant
- 1998-03-12 IL IL13187098A patent/IL131870A0/en active IP Right Grant
- 1998-03-12 SK SK1222-99A patent/SK283636B6/en not_active IP Right Cessation
- 1998-03-12 BR BR9808867-0A patent/BR9808867A/en not_active Application Discontinuation
- 1998-03-12 PL PL335672A patent/PL192786B1/en not_active IP Right Cessation
- 1998-03-12 EA EA199900823A patent/EA002378B1/en unknown
- 1998-03-12 PE PE1998000171A patent/PE58799A1/en not_active Application Discontinuation
- 1998-03-12 CN CNB988045389A patent/CN1179948C/en not_active Expired - Fee Related
- 1998-03-12 JP JP53974598A patent/JP2001516350A/en not_active Ceased
- 1998-03-12 EP EP98910300A patent/EP0970055A2/en not_active Withdrawn
- 1998-03-12 WO PCT/US1998/004735 patent/WO1998040357A2/en active IP Right Grant
- 1998-03-12 CA CA002284163A patent/CA2284163A1/en not_active Abandoned
- 1998-03-12 MY MYPI98001071A patent/MY117535A/en unknown
- 1998-03-12 GE GEAP19984984A patent/GEP20022764B/en unknown
- 1998-03-12 HU HU0001380A patent/HUP0001380A3/en unknown
- 1998-03-12 TW TW094100045A patent/TW200517112A/en unknown
- 1998-03-12 NZ NZ337706A patent/NZ337706A/en unknown
- 1998-03-12 AU AU64575/98A patent/AU743078B2/en not_active Ceased
- 1998-03-12 KR KR10-1999-7008331A patent/KR100511089B1/en not_active IP Right Cessation
- 1998-03-12 MX MXPA99008395A patent/MXPA99008395A/en not_active IP Right Cessation
- 1998-03-12 CZ CZ0319199A patent/CZ296647B6/en not_active IP Right Cessation
- 1998-03-12 TR TR1999/02508T patent/TR199902508T2/en unknown
- 1998-03-12 AP APAP/P/1999/001648A patent/AP1358A/en active
- 1998-03-12 EE EEP199900416A patent/EE04114B1/en not_active IP Right Cessation
- 1998-03-13 CO CO98014251A patent/CO4940496A1/en unknown
- 1998-03-13 SV SV1998000038A patent/SV1998000038A/en not_active Application Discontinuation
- 1998-03-13 PA PA19988448801A patent/PA8448801A1/en unknown
- 1998-04-21 SA SA98181116A patent/SA98181116B1/en unknown
- 1998-12-03 UA UA99095049A patent/UA57772C2/en unknown
-
1999
- 1999-09-10 IS IS5176A patent/IS5176A/en unknown
- 1999-09-10 NO NO19994415A patent/NO315555B1/en not_active IP Right Cessation
- 1999-09-10 IL IL131870A patent/IL131870A/en not_active IP Right Cessation
- 1999-09-13 OA OA9900207A patent/OA11196A/en unknown
- 1999-09-13 BG BG103727A patent/BG63540B1/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2287387T3 (en) | HIV PROTEASE INHIBITORS. | |
| US5527829A (en) | HIV protease inhibitors | |
| NZ250490A (en) | Hiv protease inhibitors and medicaments | |
| EP0741719A1 (en) | Intermediate and process for making | |
| US6001851A (en) | HIV protease inhibitors | |
| CA2284163A1 (en) | Hiv protease inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |